Canonical Allele Identifier: CA505120262

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679434C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679423C>G , CM000681.2:g.6679423C>G	GRCh38
NC_000019.9:g.6679434C>G , CM000681.1:g.6679434C>G	GRCh37
NC_000019.8:g.6630434C>G	NCBI36
NG_009557.1:g.46229G>C , LRG_27:g.46229G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2878G>C
ENST00000695653.1:c.2439G>C	ENSP00000512084.1:p.Leu813=
ENST00000695654.1:c.3555G>C	ENSP00000512085.1:p.Leu1185=
ENST00000695689.1:c.501G>C	ENSP00000512101.1:n.501G>C
ENST00000695690.1:n.1595G>C
ENST00000695691.1:n.1391G>C
ENST00000245907.11:c.4530G>C MANE Select	ENSP00000245907.4:p.Leu1510=
ENST00000245907.10:c.4530G>C	ENSP00000245907.4:p.Leu1510=
ENST00000599668.1:n.125G>C
ENST00000599899.5:n.1489G>C
ENST00000601008.1:c.242-1465G>C	ENSP00000471384.1:n.242-1465G>C
NM_000064.3:c.4530G>C	NP_000055.2:p.Leu1510=
NM_000064.4:c.4530G>C MANE Select	NP_000055.2:p.Leu1510=