Canonical Allele Identifier: CA2587871943

Gene: C3

Linked Data

• gnomAD v4: 19-6679602-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679602T>C , CM000681.2:g.6679602T>C	GRCh38
NC_000019.9:g.6679613T>C , CM000681.1:g.6679613T>C	GRCh37
NC_000019.8:g.6630613T>C	NCBI36
NG_009557.1:g.46050A>G , LRG_27:g.46050A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-106A>G
ENST00000695653.1:c.2366-106A>G	ENSP00000512084.1:n.2366-106A>G
ENST00000695654.1:c.3482-106A>G	ENSP00000512085.1:n.3482-106A>G
ENST00000695689.1:c.428-106A>G	ENSP00000512101.1:n.428-106A>G
ENST00000695690.1:n.1522-106A>G
ENST00000695691.1:n.1318-106A>G
ENST00000245907.11:c.4457-106A>G MANE Select	ENSP00000245907.4:n.4457-106A>G
ENST00000245907.10:c.4457-106A>G	ENSP00000245907.4:n.4457-106A>G
ENST00000599668.1:n.52-106A>G
ENST00000599899.5:n.1416-106A>G
ENST00000601008.1:c.242-1644A>G	ENSP00000471384.1:n.242-1644A>G
NM_000064.3:c.4457-106A>G	NP_000055.2:n.4457-106A>G
NM_000064.4:c.4457-106A>G MANE Select	NP_000055.2:n.4457-106A>G