Canonical Allele Identifier: CA1217904165

Gene: F13B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197039236G= , CM000663.2:g.197039236G=	GRCh38
NC_000001.10:g.197008366G= , CM000663.1:g.197008366G=	GRCh37
NC_000001.9:g.195274989G=	NCBI36
NG_012065.1:g.33032C= , LRG_550:g.33032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367412.2:c.*142C= MANE Select	ENSP00000356382.2:n.*142C=
ENST00000649282.1:c.883C=	ENSP00000497116.1:n.883C=
ENST00000367412.1:c.*142C=	ENSP00000356382.1:n.*142C=
NM_001994.2:c.*142C= , LRG_550t1:c.*142C=	NP_001985.2:n.*142C=
XM_011509283.2:c.*1063C=	XP_011507585.1:n.*1063C=
XM_011509284.2:c.*1063C=	XP_011507586.1:n.*1063C=
XM_011509286.2:c.*1063C=	XP_011507588.1:n.*1063C=
NM_001994.3:c.*142C= MANE Select	NP_001985.2:n.*142C=