Canonical Allele Identifier: CA2587871728

Gene: C3

Linked Data

• gnomAD v4: 19-6679246-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679246C>T , CM000681.2:g.6679246C>T	GRCh38
NC_000019.9:g.6679257C>T , CM000681.1:g.6679257C>T	GRCh37
NC_000019.8:g.6630257C>T	NCBI36
NG_009557.1:g.46406G>A , LRG_27:g.46406G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2895-38G>A
ENST00000695653.1:c.2456-38G>A	ENSP00000512084.1:n.2456-38G>A
ENST00000695654.1:c.3572-38G>A	ENSP00000512085.1:n.3572-38G>A
ENST00000695689.1:c.518-38G>A	ENSP00000512101.1:n.518-38G>A
ENST00000695690.1:n.1612-38G>A
ENST00000695691.1:n.1408-38G>A
ENST00000245907.11:c.4547-38G>A MANE Select	ENSP00000245907.4:n.4547-38G>A
ENST00000245907.10:c.4547-38G>A	ENSP00000245907.4:n.4547-38G>A
ENST00000599668.1:n.167-38G>A
ENST00000599899.5:n.1506-38G>A
ENST00000601008.1:c.242-1288G>A	ENSP00000471384.1:n.242-1288G>A
NM_000064.3:c.4547-38G>A	NP_000055.2:n.4547-38G>A
NM_000064.4:c.4547-38G>A MANE Select	NP_000055.2:n.4547-38G>A