Canonical Allele Identifier: CA505120647

Gene: C3

Linked Data

• gnomAD v4: 19-6679495-C-T
• MyVariant Identifiers: chr19:g.6679506C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679495C>T , CM000681.2:g.6679495C>T	GRCh38
NC_000019.9:g.6679506C>T , CM000681.1:g.6679506C>T	GRCh37
NC_000019.8:g.6630506C>T	NCBI36
NG_009557.1:g.46157G>A , LRG_27:g.46157G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2806G>A
ENST00000695653.1:c.2367G>A	ENSP00000512084.1:p.Glu789=
ENST00000695654.1:c.3483G>A	ENSP00000512085.1:p.Glu1161=
ENST00000695689.1:c.429G>A	ENSP00000512101.1:n.429G>A
ENST00000695690.1:n.1523G>A
ENST00000695691.1:n.1319G>A
ENST00000245907.11:c.4458G>A MANE Select	ENSP00000245907.4:p.Glu1486=
ENST00000245907.10:c.4458G>A	ENSP00000245907.4:p.Glu1486=
ENST00000599668.1:n.53G>A
ENST00000599899.5:n.1417G>A
ENST00000601008.1:c.242-1537G>A	ENSP00000471384.1:n.242-1537G>A
NM_000064.3:c.4458G>A	NP_000055.2:p.Glu1486=
NM_000064.4:c.4458G>A MANE Select	NP_000055.2:p.Glu1486=