Canonical Allele Identifier: CA403619391

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686151C>T (hg19) ; chr19:g.6686140C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686140C>T , CM000681.2:g.6686140C>T	GRCh38
NC_000019.9:g.6686151C>T , CM000681.1:g.6686151C>T	GRCh37
NC_000019.8:g.6637151C>T	NCBI36
NG_009557.1:g.39512G>A , LRG_27:g.39512G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2142G>A
ENST00000695652.1:c.3671G>A	ENSP00000512083.1:p.Gly1224Asp
ENST00000695653.1:c.1703G>A	ENSP00000512084.1:p.Gly568Asp
ENST00000695654.1:c.2819G>A	ENSP00000512085.1:p.Gly940Asp
ENST00000695655.1:c.2735G>A	ENSP00000512086.1:n.2735G>A
ENST00000695692.1:n.3158G>A
ENST00000245907.11:c.3794G>A MANE Select	ENSP00000245907.4:p.Gly1265Asp
ENST00000245907.10:c.3794G>A	ENSP00000245907.4:p.Gly1265Asp
ENST00000596238.1:n.237G>A
ENST00000601008.1:c.241+606G>A	ENSP00000471384.1:n.241+606G>A
NM_000064.3:c.3794G>A	NP_000055.2:p.Gly1265Asp
NM_000064.4:c.3794G>A MANE Select	NP_000055.2:p.Gly1265Asp