Canonical Allele Identifier: CA505123734

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686279G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686268G>A , CM000681.2:g.6686268G>A	GRCh38
NC_000019.9:g.6686279G>A , CM000681.1:g.6686279G>A	GRCh37
NC_000019.8:g.6637279G>A	NCBI36
NG_009557.1:g.39384C>T , LRG_27:g.39384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2014C>T
ENST00000695652.1:c.3543C>T	ENSP00000512083.1:p.Asp1181=
ENST00000695653.1:c.1575C>T	ENSP00000512084.1:p.Asp525=
ENST00000695654.1:c.2691C>T	ENSP00000512085.1:p.Asp897=
ENST00000695655.1:c.2607C>T	ENSP00000512086.1:n.2607C>T
ENST00000695692.1:n.3030C>T
ENST00000245907.11:c.3666C>T MANE Select	ENSP00000245907.4:p.Asp1222=
ENST00000245907.10:c.3666C>T	ENSP00000245907.4:p.Asp1222=
ENST00000596238.1:n.109C>T
ENST00000601008.1:c.241+478C>T	ENSP00000471384.1:n.241+478C>T
NM_000064.3:c.3666C>T	NP_000055.2:p.Asp1222=
NM_000064.4:c.3666C>T MANE Select	NP_000055.2:p.Asp1222=