Canonical Allele Identifier: CA403633429

Gene: C3

Linked Data

• dbSNP Id: rs1967565262
• gnomAD v4: 19-6697528-G-C
• MyVariant Identifiers: chr19:g.6697539G>C (hg19) ; chr19:g.6697528G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697528G>C , CM000681.2:g.6697528G>C	GRCh38
NC_000019.9:g.6697539G>C , CM000681.1:g.6697539G>C	GRCh37
NC_000019.8:g.6648539G>C	NCBI36
NG_009557.1:g.28124C>G , LRG_27:g.28124C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.960C>G
ENST00000695652.1:c.2489C>G	ENSP00000512083.1:p.Ala830Gly
ENST00000695653.1:c.521C>G	ENSP00000512084.1:p.Ala174Gly
ENST00000695654.1:c.1736C>G	ENSP00000512085.1:p.Ala579Gly
ENST00000695655.1:c.1553C>G	ENSP00000512086.1:n.1553C>G
ENST00000695692.1:n.1976C>G
ENST00000245907.11:c.2612C>G MANE Select	ENSP00000245907.4:p.Ala871Gly
ENST00000245907.10:c.2612C>G	ENSP00000245907.4:p.Ala871Gly
ENST00000594005.1:n.188C>G
NM_000064.3:c.2612C>G	NP_000055.2:p.Ala871Gly
NM_000064.4:c.2612C>G MANE Select	NP_000055.2:p.Ala871Gly