Canonical Allele Identifier: CA505123661

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686153A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686142A>T , CM000681.2:g.6686142A>T	GRCh38
NC_000019.9:g.6686153A>T , CM000681.1:g.6686153A>T	GRCh37
NC_000019.8:g.6637153A>T	NCBI36
NG_009557.1:g.39510T>A , LRG_27:g.39510T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2140T>A
ENST00000695652.1:c.3669T>A	ENSP00000512083.1:p.Gly1223=
ENST00000695653.1:c.1701T>A	ENSP00000512084.1:p.Gly567=
ENST00000695654.1:c.2817T>A	ENSP00000512085.1:p.Gly939=
ENST00000695655.1:c.2733T>A	ENSP00000512086.1:n.2733T>A
ENST00000695692.1:n.3156T>A
ENST00000245907.11:c.3792T>A MANE Select	ENSP00000245907.4:p.Gly1264=
ENST00000245907.10:c.3792T>A	ENSP00000245907.4:p.Gly1264=
ENST00000596238.1:n.235T>A
ENST00000601008.1:c.241+604T>A	ENSP00000471384.1:n.241+604T>A
NM_000064.3:c.3792T>A	NP_000055.2:p.Gly1264=
NM_000064.4:c.3792T>A MANE Select	NP_000055.2:p.Gly1264=