Canonical Allele Identifier: CA993066640

Gene: C3

Linked Data

• dbSNP Id: rs1918008878
• gnomAD v3: 19-6686326-T-C
• gnomAD v4: 19-6686326-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686326T>C , CM000681.2:g.6686326T>C	GRCh38
NC_000019.9:g.6686337T>C , CM000681.1:g.6686337T>C	GRCh37
NC_000019.8:g.6637337T>C	NCBI36
NG_009557.1:g.39326A>G , LRG_27:g.39326A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-39A>G
ENST00000695652.1:c.3524-39A>G	ENSP00000512083.1:n.3524-39A>G
ENST00000695653.1:c.1556-39A>G	ENSP00000512084.1:n.1556-39A>G
ENST00000695654.1:c.2672-39A>G	ENSP00000512085.1:n.2672-39A>G
ENST00000695655.1:c.2588-39A>G	ENSP00000512086.1:n.2588-39A>G
ENST00000695692.1:n.3011-39A>G
ENST00000245907.11:c.3647-39A>G MANE Select	ENSP00000245907.4:n.3647-39A>G
ENST00000245907.10:c.3647-39A>G	ENSP00000245907.4:n.3647-39A>G
ENST00000596238.1:n.51A>G
ENST00000598805.2:n.836A>G
ENST00000601008.1:c.241+420A>G	ENSP00000471384.1:n.241+420A>G
NM_000064.3:c.3647-39A>G	NP_000055.2:n.3647-39A>G
NM_000064.4:c.3647-39A>G MANE Select	NP_000055.2:n.3647-39A>G