Human (GRCh37.p13)
Description

family with sequence similarity 166, member B [Source:HGNC Symbol;Acc:34242]

Location

Chromosome 9: 35,561,828-35,563,896 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 5 transcripts (splice variants).

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000399742.2FAM166B-005958275aaENSP00000382646.2
 
Protein coding
CCDS56572A8MTA8 NM_001164310.1GENCODE basic
ENST00000447837.1FAM166B-004889216aaENSP00000412746.1
 
Nonsense mediated decay
CCDS47963A8MTA8 --
ENST00000492890.1FAM166B-001971No protein-
 
Processed transcript
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ENST00000480287.1FAM166B-002681No protein-
 
Processed transcript
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ENST00000478246.1FAM166B-003627No protein-
 
Processed transcript
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