Canonical Allele Identifier: CA2320553472

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686219C= , CM000681.2:g.6686219C=	GRCh38
NC_000019.9:g.6686230C= , CM000681.1:g.6686230C=	GRCh37
NC_000019.8:g.6637230C=	NCBI36
NG_009557.1:g.39433G= , LRG_27:g.39433G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2063G=
ENST00000695652.1:c.3592G=	ENSP00000512083.1:p.Ala1198=
ENST00000695653.1:c.1624G=	ENSP00000512084.1:p.Ala542=
ENST00000695654.1:c.2740G=	ENSP00000512085.1:p.Ala914=
ENST00000695655.1:c.2656G=	ENSP00000512086.1:n.2656G=
ENST00000695692.1:n.3079G=
ENST00000245907.11:c.3715G= MANE Select	ENSP00000245907.4:p.Ala1239=
ENST00000245907.10:c.3715G=	ENSP00000245907.4:p.Ala1239=
ENST00000596238.1:n.158G=
ENST00000601008.1:c.241+527G=	ENSP00000471384.1:n.241+527G=
NM_000064.3:c.3715G=	NP_000055.2:p.Ala1239=
NM_000064.4:c.3715G= MANE Select	NP_000055.2:p.Ala1239=