Canonical Allele Identifier: CA1217904196

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039327A= , CM000663.2:g.197039327A=	GRCh38
NC_000001.10:g.197008457A= , CM000663.1:g.197008457A=	GRCh37
NC_000001.9:g.195275080A=	NCBI36
NG_012065.1:g.32941T= , LRG_550:g.32941T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367412.2:c.*51T= MANE Select	ENSP00000356382.2:n.*51T=
ENST00000649282.1:c.792T=	ENSP00000497116.1:n.792T=
ENST00000367412.1:c.*51T=	ENSP00000356382.1:n.*51T=
NM_001994.2:c.*51T= , LRG_550t1:c.*51T=	NP_001985.2:n.*51T=
XM_011509283.2:c.*972T=	XP_011507585.1:n.*972T=
XM_011509284.2:c.*972T=	XP_011507586.1:n.*972T=
XM_011509286.2:c.*972T=	XP_011507588.1:n.*972T=
NM_001994.3:c.*51T= MANE Select	NP_001985.2:n.*51T=