Canonical Allele Identifier: CA1139825482

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039235C= , CM000663.2:g.197039235C=	GRCh38
NC_000001.10:g.197008365C= , CM000663.1:g.197008365C=	GRCh37
NC_000001.9:g.195274988C=	NCBI36
NG_012065.1:g.33033G= , LRG_550:g.33033G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*143G= MANE Select	ENSP00000356382.2:n.*143G=
ENST00000649282.1:c.884G=	ENSP00000497116.1:n.884G=
ENST00000367412.1:c.*143G=	ENSP00000356382.1:n.*143G=
NM_001994.2:c.*143G= , LRG_550t1:c.*143G=	NP_001985.2:n.*143G=
XM_011509283.2:c.*1064G=	XP_011507585.1:n.*1064G=
XM_011509284.2:c.*1064G=	XP_011507586.1:n.*1064G=
XM_011509286.2:c.*1064G=	XP_011507588.1:n.*1064G=
NM_001994.3:c.*143G= MANE Select	NP_001985.2:n.*143G=