Canonical Allele Identifier: CA505192439

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697672T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697661T>C , CM000681.2:g.6697661T>C	GRCh38
NC_000019.9:g.6697672T>C , CM000681.1:g.6697672T>C	GRCh37
NC_000019.8:g.6648672T>C	NCBI36
NG_009557.1:g.27991A>G , LRG_27:g.27991A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.922A>G
ENST00000695652.1:c.2451A>G	ENSP00000512083.1:p.Gln817=
ENST00000695653.1:c.483A>G	ENSP00000512084.1:p.Gln161=
ENST00000695654.1:c.1698A>G	ENSP00000512085.1:p.Gln566=
ENST00000695655.1:c.1515A>G	ENSP00000512086.1:n.1515A>G
ENST00000695692.1:n.1938A>G
ENST00000245907.11:c.2574A>G MANE Select	ENSP00000245907.4:p.Gln858=
ENST00000245907.10:c.2574A>G	ENSP00000245907.4:p.Gln858=
ENST00000594005.1:n.55A>G
NM_000064.3:c.2574A>G	NP_000055.2:p.Gln858=
NM_000064.4:c.2574A>G MANE Select	NP_000055.2:p.Gln858=