Canonical Allele Identifier: CA505192513

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697729A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697718A>T , CM000681.2:g.6697718A>T	GRCh38
NC_000019.9:g.6697729A>T , CM000681.1:g.6697729A>T	GRCh37
NC_000019.8:g.6648729A>T	NCBI36
NG_009557.1:g.27934T>A , LRG_27:g.27934T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.865T>A
ENST00000695652.1:c.2394T>A	ENSP00000512083.1:p.Val798=
ENST00000695653.1:c.426T>A	ENSP00000512084.1:p.Val142=
ENST00000695654.1:c.1641T>A	ENSP00000512085.1:p.Val547=
ENST00000695655.1:c.1458T>A	ENSP00000512086.1:n.1458T>A
ENST00000695692.1:n.1881T>A
ENST00000245907.11:c.2517T>A MANE Select	ENSP00000245907.4:p.Val839=
ENST00000245907.10:c.2517T>A	ENSP00000245907.4:p.Val839=
ENST00000602053.1:n.565T>A
NM_000064.3:c.2517T>A	NP_000055.2:p.Val839=
NM_000064.4:c.2517T>A MANE Select	NP_000055.2:p.Val839=