Canonical Allele Identifier: CA505123725

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686264G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686253G>T , CM000681.2:g.6686253G>T	GRCh38
NC_000019.9:g.6686264G>T , CM000681.1:g.6686264G>T	GRCh37
NC_000019.8:g.6637264G>T	NCBI36
NG_009557.1:g.39399C>A , LRG_27:g.39399C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2029C>A
ENST00000695652.1:c.3558C>A	ENSP00000512083.1:p.Leu1186=
ENST00000695653.1:c.1590C>A	ENSP00000512084.1:p.Leu530=
ENST00000695654.1:c.2706C>A	ENSP00000512085.1:p.Leu902=
ENST00000695655.1:c.2622C>A	ENSP00000512086.1:n.2622C>A
ENST00000695692.1:n.3045C>A
ENST00000245907.11:c.3681C>A MANE Select	ENSP00000245907.4:p.Leu1227=
ENST00000245907.10:c.3681C>A	ENSP00000245907.4:p.Leu1227=
ENST00000596238.1:n.124C>A
ENST00000601008.1:c.241+493C>A	ENSP00000471384.1:n.241+493C>A
NM_000064.3:c.3681C>A	NP_000055.2:p.Leu1227=
NM_000064.4:c.3681C>A MANE Select	NP_000055.2:p.Leu1227=