Canonical Allele Identifier: CA2320565971

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709840C= , CM000681.2:g.6709840C=	GRCh38
NC_000019.9:g.6709851C= , CM000681.1:g.6709851C=	GRCh37
NC_000019.8:g.6660851C=	NCBI36
NG_009557.1:g.15812G= , LRG_27:g.15812G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1566G=	ENSP00000512083.1:p.Leu522=
ENST00000695654.1:c.813G=	ENSP00000512085.1:p.Leu271=
ENST00000695655.1:c.630G=	ENSP00000512086.1:n.630G=
ENST00000695692.1:n.1053G=
ENST00000245907.11:c.1689G= MANE Select	ENSP00000245907.4:p.Leu563=
ENST00000245907.10:c.1689G=	ENSP00000245907.4:p.Leu563=
ENST00000600763.1:n.322G=
NM_000064.3:c.1689G=	NP_000055.2:p.Leu563=
NM_000064.4:c.1689G= MANE Select	NP_000055.2:p.Leu563=