Canonical Allele Identifier: CA505120334

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679449G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679438G>C , CM000681.2:g.6679438G>C	GRCh38
NC_000019.9:g.6679449G>C , CM000681.1:g.6679449G>C	GRCh37
NC_000019.8:g.6630449G>C	NCBI36
NG_009557.1:g.46214C>G , LRG_27:g.46214C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2863C>G
ENST00000695653.1:c.2424C>G	ENSP00000512084.1:p.Leu808=
ENST00000695654.1:c.3540C>G	ENSP00000512085.1:p.Leu1180=
ENST00000695689.1:c.486C>G	ENSP00000512101.1:n.486C>G
ENST00000695690.1:n.1580C>G
ENST00000695691.1:n.1376C>G
ENST00000245907.11:c.4515C>G MANE Select	ENSP00000245907.4:p.Leu1505=
ENST00000245907.10:c.4515C>G	ENSP00000245907.4:p.Leu1505=
ENST00000599668.1:n.110C>G
ENST00000599899.5:n.1474C>G
ENST00000601008.1:c.242-1480C>G	ENSP00000471384.1:n.242-1480C>G
NM_000064.3:c.4515C>G	NP_000055.2:p.Leu1505=
NM_000064.4:c.4515C>G MANE Select	NP_000055.2:p.Leu1505=