Canonical Allele Identifier: CA1142334786

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039385C= , CM000663.2:g.197039385C=	GRCh38
NC_000001.10:g.197008515C= , CM000663.1:g.197008515C=	GRCh37
NC_000001.9:g.195275138C=	NCBI36
NG_012065.1:g.32883G= , LRG_550:g.32883G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.1979G= MANE Select	ENSP00000356382.2:p.Arg660=
ENST00000649282.1:c.734G=	ENSP00000497116.1:p.Arg245=
ENST00000367412.1:c.1979G=	ENSP00000356382.1:p.Arg660=
NM_001994.2:c.1979G= , LRG_550t1:c.1979G=	NP_001985.2:p.Arg660=
XM_011509283.2:c.*914G=	XP_011507585.1:n.*914G=
XM_011509284.2:c.*914G=	XP_011507586.1:n.*914G=
XM_011509286.2:c.*914G=	XP_011507588.1:n.*914G=
NM_001994.3:c.1979G= MANE Select	NP_001985.2:p.Arg660=