Canonical Allele Identifier: CA505123641

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686138G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686127G>A , CM000681.2:g.6686127G>A	GRCh38
NC_000019.9:g.6686138G>A , CM000681.1:g.6686138G>A	GRCh37
NC_000019.8:g.6637138G>A	NCBI36
NG_009557.1:g.39525C>T , LRG_27:g.39525C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2155C>T
ENST00000695652.1:c.3684C>T	ENSP00000512083.1:p.Thr1228=
ENST00000695653.1:c.1716C>T	ENSP00000512084.1:p.Thr572=
ENST00000695654.1:c.2832C>T	ENSP00000512085.1:p.Thr944=
ENST00000695655.1:c.2748C>T	ENSP00000512086.1:n.2748C>T
ENST00000695692.1:n.3171C>T
ENST00000245907.11:c.3807C>T MANE Select	ENSP00000245907.4:p.Thr1269=
ENST00000245907.10:c.3807C>T	ENSP00000245907.4:p.Thr1269=
ENST00000596238.1:n.250C>T
ENST00000601008.1:c.241+619C>T	ENSP00000471384.1:n.241+619C>T
NM_000064.3:c.3807C>T	NP_000055.2:p.Thr1269=
NM_000064.4:c.3807C>T MANE Select	NP_000055.2:p.Thr1269=