Canonical Allele Identifier: CA1217904194

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039326T= , CM000663.2:g.197039326T=	GRCh38
NC_000001.10:g.197008456T= , CM000663.1:g.197008456T=	GRCh37
NC_000001.9:g.195275079T=	NCBI36
NG_012065.1:g.32942A= , LRG_550:g.32942A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.*52A= MANE Select	ENSP00000356382.2:n.*52A=
ENST00000649282.1:c.793A=	ENSP00000497116.1:n.793A=
ENST00000367412.1:c.*52A=	ENSP00000356382.1:n.*52A=
NM_001994.2:c.*52A= , LRG_550t1:c.*52A=	NP_001985.2:n.*52A=
XM_011509283.2:c.*973A=	XP_011507585.1:n.*973A=
XM_011509284.2:c.*973A=	XP_011507586.1:n.*973A=
XM_011509286.2:c.*973A=	XP_011507588.1:n.*973A=
NM_001994.3:c.*52A= MANE Select	NP_001985.2:n.*52A=