Canonical Allele Identifier: CA505123676

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686183A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686172A>T , CM000681.2:g.6686172A>T	GRCh38
NC_000019.9:g.6686183A>T , CM000681.1:g.6686183A>T	GRCh37
NC_000019.8:g.6637183A>T	NCBI36
NG_009557.1:g.39480T>A , LRG_27:g.39480T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2110T>A
ENST00000695652.1:c.3639T>A	ENSP00000512083.1:p.Arg1213=
ENST00000695653.1:c.1671T>A	ENSP00000512084.1:p.Arg557=
ENST00000695654.1:c.2787T>A	ENSP00000512085.1:p.Arg929=
ENST00000695655.1:c.2703T>A	ENSP00000512086.1:n.2703T>A
ENST00000695692.1:n.3126T>A
ENST00000245907.11:c.3762T>A MANE Select	ENSP00000245907.4:p.Arg1254=
ENST00000245907.10:c.3762T>A	ENSP00000245907.4:p.Arg1254=
ENST00000596238.1:n.205T>A
ENST00000601008.1:c.241+574T>A	ENSP00000471384.1:n.241+574T>A
NM_000064.3:c.3762T>A	NP_000055.2:p.Arg1254=
NM_000064.4:c.3762T>A MANE Select	NP_000055.2:p.Arg1254=