Canonical Allele Identifier: CA1217904198

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039333T= , CM000663.2:g.197039333T=	GRCh38
NC_000001.10:g.197008463T= , CM000663.1:g.197008463T=	GRCh37
NC_000001.9:g.195275086T=	NCBI36
NG_012065.1:g.32935A= , LRG_550:g.32935A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.*45A= MANE Select	ENSP00000356382.2:n.*45A=
ENST00000649282.1:c.786A=	ENSP00000497116.1:n.786A=
ENST00000367412.1:c.*45A=	ENSP00000356382.1:n.*45A=
NM_001994.2:c.*45A= , LRG_550t1:c.*45A=	NP_001985.2:n.*45A=
XM_011509283.2:c.*966A=	XP_011507585.1:n.*966A=
XM_011509284.2:c.*966A=	XP_011507586.1:n.*966A=
XM_011509286.2:c.*966A=	XP_011507588.1:n.*966A=
NM_001994.3:c.*45A= MANE Select	NP_001985.2:n.*45A=