Human (GRCh37.p13)
Description

coagulation factor IX [Source:HGNC Symbol;Acc:3551]

Gene Synonyms

FIX, HEMB, P19, PTC, THPH8

Location

Chromosome X: 138,612,917-138,645,617 forward strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants), 12 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000218099.2F9-0012780461aaENSP00000218099.2
 
Protein coding
CCDS14666P00740 Q19UG6 Q19UH6
Q19UI2 Q19UK3 Q19UK4
Q19UK5 Q19UK7 Q19UL6
Q86XR9
NM_000133.3Ensembl CanonicalGENCODE Basic
ENST00000394090.2F9-2011272423aaENSP00000377650.2
 
Protein coding
P00740 Q19UG6 Q19UH6
Q19UI2 Q19UK3 Q19UK4
Q19UK5 Q19UK7 Q19UL6
Q86XR9
-GENCODE Basic
ENST00000479617.2F9-002374No protein-
 
Processed transcript
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