Canonical Allele Identifier: CA403619418

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686155C>G (hg19) ; chr19:g.6686144C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686144C>G , CM000681.2:g.6686144C>G	GRCh38
NC_000019.9:g.6686155C>G , CM000681.1:g.6686155C>G	GRCh37
NC_000019.8:g.6637155C>G	NCBI36
NG_009557.1:g.39508G>C , LRG_27:g.39508G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2138G>C
ENST00000695652.1:c.3667G>C	ENSP00000512083.1:p.Gly1223Arg
ENST00000695653.1:c.1699G>C	ENSP00000512084.1:p.Gly567Arg
ENST00000695654.1:c.2815G>C	ENSP00000512085.1:p.Gly939Arg
ENST00000695655.1:c.2731G>C	ENSP00000512086.1:n.2731G>C
ENST00000695692.1:n.3154G>C
ENST00000245907.11:c.3790G>C MANE Select	ENSP00000245907.4:p.Gly1264Arg
ENST00000245907.10:c.3790G>C	ENSP00000245907.4:p.Gly1264Arg
ENST00000596238.1:n.233G>C
ENST00000601008.1:c.241+602G>C	ENSP00000471384.1:n.241+602G>C
NM_000064.3:c.3790G>C	NP_000055.2:p.Gly1264Arg
NM_000064.4:c.3790G>C MANE Select	NP_000055.2:p.Gly1264Arg