Canonical Allele Identifier: CA403611988

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679144A>T (hg19) ; chr19:g.6679133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679133A>T , CM000681.2:g.6679133A>T	GRCh38
NC_000019.9:g.6679144A>T , CM000681.1:g.6679144A>T	GRCh37
NC_000019.8:g.6630144A>T	NCBI36
NG_009557.1:g.46519T>A , LRG_27:g.46519T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2970T>A
ENST00000695653.1:c.2531T>A	ENSP00000512084.1:p.Val844Glu
ENST00000695654.1:c.3647T>A	ENSP00000512085.1:p.Val1216Glu
ENST00000695689.1:c.593T>A	ENSP00000512101.1:n.593T>A
ENST00000695690.1:n.1687T>A
ENST00000695691.1:n.1483T>A
ENST00000245907.11:c.4622T>A MANE Select	ENSP00000245907.4:p.Val1541Glu
ENST00000245907.10:c.4622T>A	ENSP00000245907.4:p.Val1541Glu
ENST00000599668.1:n.242T>A
ENST00000599899.5:n.1581T>A
ENST00000601008.1:c.242-1175T>A	ENSP00000471384.1:n.242-1175T>A
ENST00000602229.1:c.69T>A
NM_000064.3:c.4622T>A	NP_000055.2:p.Val1541Glu
NM_000064.4:c.4622T>A MANE Select	NP_000055.2:p.Val1541Glu