Canonical Allele Identifier: CA2320559077

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697471G= , CM000681.2:g.6697471G=	GRCh38
NC_000019.9:g.6697482G= , CM000681.1:g.6697482G=	GRCh37
NC_000019.8:g.6648482G=	NCBI36
NG_009557.1:g.28181C= , LRG_27:g.28181C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1017C=
ENST00000695652.1:c.2546C=	ENSP00000512083.1:p.Pro849=
ENST00000695653.1:c.578C=	ENSP00000512084.1:p.Pro193=
ENST00000695654.1:c.1793C=	ENSP00000512085.1:p.Pro598=
ENST00000695655.1:c.1610C=	ENSP00000512086.1:n.1610C=
ENST00000695692.1:n.2033C=
ENST00000245907.11:c.2669C= MANE Select	ENSP00000245907.4:p.Pro890=
ENST00000245907.10:c.2669C=	ENSP00000245907.4:p.Pro890=
ENST00000594005.1:n.245C=
NM_000064.3:c.2669C=	NP_000055.2:p.Pro890=
NM_000064.4:c.2669C= MANE Select	NP_000055.2:p.Pro890=