Canonical Allele Identifier: CA1217904192

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039325A= , CM000663.2:g.197039325A=	GRCh38
NC_000001.10:g.197008455A= , CM000663.1:g.197008455A=	GRCh37
NC_000001.9:g.195275078A=	NCBI36
NG_012065.1:g.32943T= , LRG_550:g.32943T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.*53T= MANE Select	ENSP00000356382.2:n.*53T=
ENST00000649282.1:c.794T=	ENSP00000497116.1:n.794T=
ENST00000367412.1:c.*53T=	ENSP00000356382.1:n.*53T=
NM_001994.2:c.*53T= , LRG_550t1:c.*53T=	NP_001985.2:n.*53T=
XM_011509283.2:c.*974T=	XP_011507585.1:n.*974T=
XM_011509284.2:c.*974T=	XP_011507586.1:n.*974T=
XM_011509286.2:c.*974T=	XP_011507588.1:n.*974T=
NM_001994.3:c.*53T= MANE Select	NP_001985.2:n.*53T=