Canonical Allele Identifier: CA2320565908

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709686T= , CM000681.2:g.6709686T=	GRCh38
NC_000019.9:g.6709697T= , CM000681.1:g.6709697T=	GRCh37
NC_000019.8:g.6660697T=	NCBI36
NG_009557.1:g.15966A= , LRG_27:g.15966A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1720A=	ENSP00000512083.1:p.Lys574=
ENST00000695654.1:c.967A=	ENSP00000512085.1:p.Lys323=
ENST00000695655.1:c.784A=	ENSP00000512086.1:n.784A=
ENST00000695692.1:n.1207A=
ENST00000245907.11:c.1843A= MANE Select	ENSP00000245907.4:p.Lys615=
ENST00000245907.10:c.1843A=	ENSP00000245907.4:p.Lys615=
NM_000064.3:c.1843A=	NP_000055.2:p.Lys615=
NM_000064.4:c.1843A= MANE Select	NP_000055.2:p.Lys615=