Canonical Allele Identifier: CA505123657

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686150G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686139G>C , CM000681.2:g.6686139G>C	GRCh38
NC_000019.9:g.6686150G>C , CM000681.1:g.6686150G>C	GRCh37
NC_000019.8:g.6637150G>C	NCBI36
NG_009557.1:g.39513C>G , LRG_27:g.39513C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2143C>G
ENST00000695652.1:c.3672C>G	ENSP00000512083.1:p.Gly1224=
ENST00000695653.1:c.1704C>G	ENSP00000512084.1:p.Gly568=
ENST00000695654.1:c.2820C>G	ENSP00000512085.1:p.Gly940=
ENST00000695655.1:c.2736C>G	ENSP00000512086.1:n.2736C>G
ENST00000695692.1:n.3159C>G
ENST00000245907.11:c.3795C>G MANE Select	ENSP00000245907.4:p.Gly1265=
ENST00000245907.10:c.3795C>G	ENSP00000245907.4:p.Gly1265=
ENST00000596238.1:n.238C>G
ENST00000601008.1:c.241+607C>G	ENSP00000471384.1:n.241+607C>G
NM_000064.3:c.3795C>G	NP_000055.2:p.Gly1265=
NM_000064.4:c.3795C>G MANE Select	NP_000055.2:p.Gly1265=