Human (GRCh38.p14)
Description

coagulation factor II, thrombin [Source:HGNC Symbol;Acc:HGNC:3535]

Location

Chromosome 11: 46,719,196-46,739,506 forward strand.

GRCh38:CM000673.2

About this gene

This gene has 5 transcripts (splice variants), 85 orthologues, 1 paralogue and is associated with 7 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000311907.10F2-2011990622aaENSP00000308541.5
 
Protein coding
CCDS31476P00734 NM_000506.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000530231.5F2-2051849583aaENSP00000433907.1
 
Protein coding
E9PIT3 -GENCODE basicTSL:5
ENST00000442468.1F2-2021031324aaENSP00000387413.1
 
Protein coding
C9JV37 -TSL:3CDS 3' incomplete
ENST00000469189.1F2-203610No protein-
 
Retained intron
--TSL:2
ENST00000490274.1F2-204545No protein-
 
Retained intron
--TSL:3