Canonical Allele Identifier: CA1217904218

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039393T= , CM000663.2:g.197039393T=	GRCh38
NC_000001.10:g.197008523T= , CM000663.1:g.197008523T=	GRCh37
NC_000001.9:g.195275146T=	NCBI36
NG_012065.1:g.32875A= , LRG_550:g.32875A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.1971A= MANE Select	ENSP00000356382.2:p.Glu657=
ENST00000649282.1:c.726A=	ENSP00000497116.1:p.Glu242=
ENST00000367412.1:c.1971A=	ENSP00000356382.1:p.Glu657=
NM_001994.2:c.1971A= , LRG_550t1:c.1971A=	NP_001985.2:p.Glu657=
XM_011509283.2:c.*906A=	XP_011507585.1:n.*906A=
XM_011509284.2:c.*906A=	XP_011507586.1:n.*906A=
XM_011509286.2:c.*906A=	XP_011507588.1:n.*906A=
NM_001994.3:c.1971A= MANE Select	NP_001985.2:p.Glu657=