Human (GRCh38.p14)
Description

coagulation factor XIII B chain [Source:HGNC Symbol;Acc:HGNC:3534]

Gene Synonyms

FXIIIB

Location

Chromosome 1: 197,038,737-197,067,260 reverse strand.

GRCh38:CM000663.2

View alleles of this gene on alternative sequences

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele, 252 orthologues, 39 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367412.2F13B-2012660661aaENSP00000356382.2
 
Protein coding
CCDS1388P05160 NM_001994.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000895399.1F13B-2042459594aaENSP00000565458.1
 
Protein coding
--GENCODE Basic
ENST00000895402.1F13B-2072247533aaENSP00000565461.1
 
Protein coding
--GENCODE Basic
ENST00000895401.1F13B-2062052465aaENSP00000565460.1
 
Protein coding
--GENCODE Basic
ENST00000895404.1F13B-2092017600aaENSP00000565463.1
 
Protein coding
--GENCODE Basic
ENST00000649282.1F13B-2031378246aaENSP00000497116.1
 
Protein coding
A0A3B3IS66 -CDS 5' incomplete
ENST00000895400.1F13B-2051161164aaENSP00000565459.1
 
Protein coding
--GENCODE Basic
ENST00000895403.1F13B-208536103aaENSP00000565462.1
 
Protein coding
--GENCODE Basic
ENST00000490002.1F13B-202596No protein-
 
Protein coding CDS not defined
--TSL:3