Canonical Allele Identifier: CA2320553456

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686180C= , CM000681.2:g.6686180C=	GRCh38
NC_000019.9:g.6686191C= , CM000681.1:g.6686191C=	GRCh37
NC_000019.8:g.6637191C=	NCBI36
NG_009557.1:g.39472G= , LRG_27:g.39472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2102G=
ENST00000695652.1:c.3631G=	ENSP00000512083.1:p.Val1211=
ENST00000695653.1:c.1663G=	ENSP00000512084.1:p.Val555=
ENST00000695654.1:c.2779G=	ENSP00000512085.1:p.Val927=
ENST00000695655.1:c.2695G=	ENSP00000512086.1:n.2695G=
ENST00000695692.1:n.3118G=
ENST00000245907.11:c.3754G= MANE Select	ENSP00000245907.4:p.Val1252=
ENST00000245907.10:c.3754G=	ENSP00000245907.4:p.Val1252=
ENST00000596238.1:n.197G=
ENST00000601008.1:c.241+566G=	ENSP00000471384.1:n.241+566G=
NM_000064.3:c.3754G=	NP_000055.2:p.Val1252=
NM_000064.4:c.3754G= MANE Select	NP_000055.2:p.Val1252=