Canonical Allele Identifier: CA9128670

Gene: C3

Linked Data

• dbSNP Id: rs753860028
• ExAC: 19:6686314 C / G
• gnomAD v2: 19-6686314-C-G
• MyVariant Identifiers: chr19:g.6686314C>G (hg19) ; chr19:g.6686303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686303C>G , CM000681.2:g.6686303C>G	GRCh38
NC_000019.9:g.6686314C>G , CM000681.1:g.6686314C>G	GRCh37
NC_000019.8:g.6637314C>G	NCBI36
NG_009557.1:g.39349G>C , LRG_27:g.39349G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-16G>C
ENST00000695652.1:c.3524-16G>C	ENSP00000512083.1:n.3524-16G>C
ENST00000695653.1:c.1556-16G>C	ENSP00000512084.1:n.1556-16G>C
ENST00000695654.1:c.2672-16G>C	ENSP00000512085.1:n.2672-16G>C
ENST00000695655.1:c.2588-16G>C	ENSP00000512086.1:n.2588-16G>C
ENST00000695692.1:n.3011-16G>C
ENST00000245907.11:c.3647-16G>C MANE Select	ENSP00000245907.4:n.3647-16G>C
ENST00000245907.10:c.3647-16G>C	ENSP00000245907.4:n.3647-16G>C
ENST00000596238.1:n.74G>C
ENST00000598805.2:n.859G>C
ENST00000601008.1:c.241+443G>C	ENSP00000471384.1:n.241+443G>C
NM_000064.3:c.3647-16G>C	NP_000055.2:n.3647-16G>C
NM_000064.4:c.3647-16G>C MANE Select	NP_000055.2:n.3647-16G>C