Canonical Allele Identifier: CA403639604

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709837C>T (hg19) ; chr19:g.6709826C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709826C>T , CM000681.2:g.6709826C>T	GRCh38
NC_000019.9:g.6709837C>T , CM000681.1:g.6709837C>T	GRCh37
NC_000019.8:g.6660837C>T	NCBI36
NG_009557.1:g.15826G>A , LRG_27:g.15826G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1580G>A	ENSP00000512083.1:p.Gly527Asp
ENST00000695654.1:c.827G>A	ENSP00000512085.1:p.Gly276Asp
ENST00000695655.1:c.644G>A	ENSP00000512086.1:n.644G>A
ENST00000695692.1:n.1067G>A
ENST00000245907.11:c.1703G>A MANE Select	ENSP00000245907.4:p.Gly568Asp
ENST00000245907.10:c.1703G>A	ENSP00000245907.4:p.Gly568Asp
ENST00000600763.1:n.336G>A
NM_000064.3:c.1703G>A	NP_000055.2:p.Gly568Asp
NM_000064.4:c.1703G>A MANE Select	NP_000055.2:p.Gly568Asp