Canonical Allele Identifier: CA1217904157

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039196C= , CM000663.2:g.197039196C=	GRCh38
NC_000001.10:g.197008326C= , CM000663.1:g.197008326C=	GRCh37
NC_000001.9:g.195274949C=	NCBI36
NG_012065.1:g.33072G= , LRG_550:g.33072G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*182G= MANE Select	ENSP00000356382.2:n.*182G=
ENST00000649282.1:c.923G=	ENSP00000497116.1:n.923G=
ENST00000367412.1:c.*182G=	ENSP00000356382.1:n.*182G=
NM_001994.2:c.*182G= , LRG_550t1:c.*182G=	NP_001985.2:n.*182G=
XM_011509283.2:c.*1103G=	XP_011507585.1:n.*1103G=
XM_011509284.2:c.*1103G=	XP_011507586.1:n.*1103G=
XM_011509286.2:c.*1103G=	XP_011507588.1:n.*1103G=
NM_001994.3:c.*182G= MANE Select	NP_001985.2:n.*182G=