Canonical Allele Identifier: CA505192470

Gene: C3

Linked Data

• gnomAD v4: 19-6697688-G-C
• MyVariant Identifiers: chr19:g.6697699G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697688G>C , CM000681.2:g.6697688G>C	GRCh38
NC_000019.9:g.6697699G>C , CM000681.1:g.6697699G>C	GRCh37
NC_000019.8:g.6648699G>C	NCBI36
NG_009557.1:g.27964C>G , LRG_27:g.27964C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.895C>G
ENST00000695652.1:c.2424C>G	ENSP00000512083.1:p.Ala808=
ENST00000695653.1:c.456C>G	ENSP00000512084.1:p.Ala152=
ENST00000695654.1:c.1671C>G	ENSP00000512085.1:p.Ala557=
ENST00000695655.1:c.1488C>G	ENSP00000512086.1:n.1488C>G
ENST00000695692.1:n.1911C>G
ENST00000245907.11:c.2547C>G MANE Select	ENSP00000245907.4:p.Ala849=
ENST00000245907.10:c.2547C>G	ENSP00000245907.4:p.Ala849=
ENST00000594005.1:n.28C>G
ENST00000602053.1:n.595C>G
NM_000064.3:c.2547C>G	NP_000055.2:p.Ala849=
NM_000064.4:c.2547C>G MANE Select	NP_000055.2:p.Ala849=