Canonical Allele Identifier: CA505123590

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685143C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685132C>T , CM000681.2:g.6685132C>T	GRCh38
NC_000019.9:g.6685143C>T , CM000681.1:g.6685143C>T	GRCh37
NC_000019.8:g.6636143C>T	NCBI36
NG_009557.1:g.40520G>A , LRG_27:g.40520G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2173G>A
ENST00000695653.1:c.1734G>A	ENSP00000512084.1:p.Val578=
ENST00000695654.1:c.2850G>A	ENSP00000512085.1:p.Val950=
ENST00000695690.1:n.16G>A
ENST00000695691.1:n.16G>A
ENST00000245907.11:c.3825G>A MANE Select	ENSP00000245907.4:p.Val1275=
ENST00000245907.10:c.3825G>A	ENSP00000245907.4:p.Val1275=
ENST00000596238.1:n.268G>A
ENST00000601008.1:c.241+1614G>A	ENSP00000471384.1:n.241+1614G>A
NM_000064.3:c.3825G>A	NP_000055.2:p.Val1275=
NM_000064.4:c.3825G>A MANE Select	NP_000055.2:p.Val1275=