Canonical Allele Identifier: CA1168786769

Gene: C8B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.56956809T= , CM000663.2:g.56956809T=	GRCh38
NC_000001.10:g.57422482T= , CM000663.1:g.57422482T=	GRCh37
NC_000001.9:g.57195070T=	NCBI36
NG_007285.1:g.14207A= , LRG_31:g.14207A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468990.2:c.*192A=	ENSP00000512215.1:n.*192A=
ENST00000494324.2:c.*456A=	ENSP00000512216.1:n.*456A=
ENST00000695842.1:c.351A=	ENSP00000512214.1:p.Gly117=
ENST00000695843.1:c.*192A=	ENSP00000512217.1:n.*192A=
ENST00000696144.1:c.351A=	ENSP00000512436.1:p.Gly117=
ENST00000696164.1:c.351A=	ENSP00000512454.1:p.Gly117=
ENST00000696165.1:c.*192A=	ENSP00000512455.1:n.*192A=
ENST00000696166.1:c.*192A=	ENSP00000512456.1:n.*192A=
ENST00000371237.9:c.351A= MANE Select	ENSP00000360281.4:p.Gly117=
ENST00000371237.8:c.351A=	ENSP00000360281.4:p.Gly117=
ENST00000535057.5:c.165A=	ENSP00000440113.1:p.Gly55=
ENST00000543257.5:c.195A=	ENSP00000442548.1:p.Gly65=
NM_000066.3:c.351A=	NP_000057.2:p.Arg117=
NM_001278543.1:c.195A=	NP_001265472.1:p.Arg65=
NM_001278544.1:c.165A=	NP_001265473.1:p.Arg55=
XM_017002235.1:c.351A=	XP_016857724.1:p.Gly117=
XR_001737397.1:n.451A=
NM_000066.4:c.351A= MANE Select	NP_000057.3:p.Gly117=
NM_001278543.2:c.195A=	NP_001265472.2:p.Gly65=
NM_001278544.2:c.165A=	NP_001265473.2:p.Gly55=