Canonical Allele Identifier: CA1217904177

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039280G= , CM000663.2:g.197039280G=	GRCh38
NC_000001.10:g.197008410G= , CM000663.1:g.197008410G=	GRCh37
NC_000001.9:g.195275033G=	NCBI36
NG_012065.1:g.32988C= , LRG_550:g.32988C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*98C= MANE Select	ENSP00000356382.2:n.*98C=
ENST00000649282.1:c.839C=	ENSP00000497116.1:n.839C=
ENST00000367412.1:c.*98C=	ENSP00000356382.1:n.*98C=
NM_001994.2:c.*98C= , LRG_550t1:c.*98C=	NP_001985.2:n.*98C=
XM_011509283.2:c.*1019C=	XP_011507585.1:n.*1019C=
XM_011509284.2:c.*1019C=	XP_011507586.1:n.*1019C=
XM_011509286.2:c.*1019C=	XP_011507588.1:n.*1019C=
NM_001994.3:c.*98C= MANE Select	NP_001985.2:n.*98C=