Canonical Allele Identifier: CA2320559217

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697780C= , CM000681.2:g.6697780C=	GRCh38
NC_000019.9:g.6697791C= , CM000681.1:g.6697791C=	GRCh37
NC_000019.8:g.6648791C=	NCBI36
NG_009557.1:g.27872G= , LRG_27:g.27872G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.803G=
ENST00000695652.1:c.2332G=	ENSP00000512083.1:p.Asp778=
ENST00000695653.1:c.364G=	ENSP00000512084.1:p.Asp122=
ENST00000695654.1:c.1579G=	ENSP00000512085.1:p.Asp527=
ENST00000695655.1:c.1396G=	ENSP00000512086.1:n.1396G=
ENST00000695692.1:n.1819G=
ENST00000245907.11:c.2455G= MANE Select	ENSP00000245907.4:p.Asp819=
ENST00000245907.10:c.2455G=	ENSP00000245907.4:p.Asp819=
ENST00000602053.1:n.503G=
NM_000064.3:c.2455G=	NP_000055.2:p.Asp819=
NM_000064.4:c.2455G= MANE Select	NP_000055.2:p.Asp819=