Canonical Allele Identifier: CA403620312

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686297A>T (hg19) ; chr19:g.6686286A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686286A>T , CM000681.2:g.6686286A>T	GRCh38
NC_000019.9:g.6686297A>T , CM000681.1:g.6686297A>T	GRCh37
NC_000019.8:g.6637297A>T	NCBI36
NG_009557.1:g.39366T>A , LRG_27:g.39366T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1996T>A
ENST00000695652.1:c.3525T>A	ENSP00000512083.1:p.Asp1175Glu
ENST00000695653.1:c.1557T>A	ENSP00000512084.1:p.Asp519Glu
ENST00000695654.1:c.2673T>A	ENSP00000512085.1:p.Asp891Glu
ENST00000695655.1:c.2589T>A	ENSP00000512086.1:n.2589T>A
ENST00000695692.1:n.3012T>A
ENST00000245907.11:c.3648T>A MANE Select	ENSP00000245907.4:p.Asp1216Glu
ENST00000245907.10:c.3648T>A	ENSP00000245907.4:p.Asp1216Glu
ENST00000596238.1:n.91T>A
ENST00000601008.1:c.241+460T>A	ENSP00000471384.1:n.241+460T>A
NM_000064.3:c.3648T>A	NP_000055.2:p.Asp1216Glu
NM_000064.4:c.3648T>A MANE Select	NP_000055.2:p.Asp1216Glu