Canonical Allele Identifier: CA9128669

Gene: C3

Linked Data

• dbSNP Id: rs764295765
• ExAC: 19:6686312 A / G
• gnomAD v2: 19-6686312-A-G
• MyVariant Identifiers: chr19:g.6686312A>G (hg19) ; chr19:g.6686301A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686301A>G , CM000681.2:g.6686301A>G	GRCh38
NC_000019.9:g.6686312A>G , CM000681.1:g.6686312A>G	GRCh37
NC_000019.8:g.6637312A>G	NCBI36
NG_009557.1:g.39351T>C , LRG_27:g.39351T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1995-14T>C
ENST00000695652.1:c.3524-14T>C	ENSP00000512083.1:n.3524-14T>C
ENST00000695653.1:c.1556-14T>C	ENSP00000512084.1:n.1556-14T>C
ENST00000695654.1:c.2672-14T>C	ENSP00000512085.1:n.2672-14T>C
ENST00000695655.1:c.2588-14T>C	ENSP00000512086.1:n.2588-14T>C
ENST00000695692.1:n.3011-14T>C
ENST00000245907.11:c.3647-14T>C MANE Select	ENSP00000245907.4:n.3647-14T>C
ENST00000245907.10:c.3647-14T>C	ENSP00000245907.4:n.3647-14T>C
ENST00000596238.1:n.76T>C
ENST00000598805.2:n.861T>C
ENST00000601008.1:c.241+445T>C	ENSP00000471384.1:n.241+445T>C
NM_000064.3:c.3647-14T>C	NP_000055.2:n.3647-14T>C
NM_000064.4:c.3647-14T>C MANE Select	NP_000055.2:n.3647-14T>C