Canonical Allele Identifier: CA884132398

Gene: C3

Linked Data

• dbSNP Id: rs1315011041
• gnomAD v4: 19-6686325-C-T
• MyVariant Identifiers: chr19:g.6686336C>T (hg19) ; chr19:g.6686325C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686325C>T , CM000681.2:g.6686325C>T	GRCh38
NC_000019.9:g.6686336C>T , CM000681.1:g.6686336C>T	GRCh37
NC_000019.8:g.6637336C>T	NCBI36
NG_009557.1:g.39327G>A , LRG_27:g.39327G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-38G>A
ENST00000695652.1:c.3524-38G>A	ENSP00000512083.1:n.3524-38G>A
ENST00000695653.1:c.1556-38G>A	ENSP00000512084.1:n.1556-38G>A
ENST00000695654.1:c.2672-38G>A	ENSP00000512085.1:n.2672-38G>A
ENST00000695655.1:c.2588-38G>A	ENSP00000512086.1:n.2588-38G>A
ENST00000695692.1:n.3011-38G>A
ENST00000245907.11:c.3647-38G>A MANE Select	ENSP00000245907.4:n.3647-38G>A
ENST00000245907.10:c.3647-38G>A	ENSP00000245907.4:n.3647-38G>A
ENST00000596238.1:n.52G>A
ENST00000598805.2:n.837G>A
ENST00000601008.1:c.241+421G>A	ENSP00000471384.1:n.241+421G>A
NM_000064.3:c.3647-38G>A	NP_000055.2:n.3647-38G>A
NM_000064.4:c.3647-38G>A MANE Select	NP_000055.2:n.3647-38G>A