Canonical Allele Identifier: CA505124517

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697804C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697793C>G , CM000681.2:g.6697793C>G	GRCh38
NC_000019.9:g.6697804C>G , CM000681.1:g.6697804C>G	GRCh37
NC_000019.8:g.6648804C>G	NCBI36
NG_009557.1:g.27859G>C , LRG_27:g.27859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.790G>C
ENST00000695652.1:c.2319G>C	ENSP00000512083.1:p.Gly773=
ENST00000695653.1:c.351G>C	ENSP00000512084.1:p.Gly117=
ENST00000695654.1:c.1566G>C	ENSP00000512085.1:p.Gly522=
ENST00000695655.1:c.1383G>C	ENSP00000512086.1:n.1383G>C
ENST00000695692.1:n.1806G>C
ENST00000245907.11:c.2442G>C MANE Select	ENSP00000245907.4:p.Gly814=
ENST00000245907.10:c.2442G>C	ENSP00000245907.4:p.Gly814=
ENST00000602053.1:n.490G>C
NM_000064.3:c.2442G>C	NP_000055.2:p.Gly814=
NM_000064.4:c.2442G>C MANE Select	NP_000055.2:p.Gly814=