Canonical Allele Identifier: CA505119935

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679152C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679141C>T , CM000681.2:g.6679141C>T	GRCh38
NC_000019.9:g.6679152C>T , CM000681.1:g.6679152C>T	GRCh37
NC_000019.8:g.6630152C>T	NCBI36
NG_009557.1:g.46511G>A , LRG_27:g.46511G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2962G>A
ENST00000695653.1:c.2523G>A	ENSP00000512084.1:p.Glu841=
ENST00000695654.1:c.3639G>A	ENSP00000512085.1:p.Glu1213=
ENST00000695689.1:c.585G>A	ENSP00000512101.1:n.585G>A
ENST00000695690.1:n.1679G>A
ENST00000695691.1:n.1475G>A
ENST00000245907.11:c.4614G>A MANE Select	ENSP00000245907.4:p.Glu1538=
ENST00000245907.10:c.4614G>A	ENSP00000245907.4:p.Glu1538=
ENST00000599668.1:n.234G>A
ENST00000599899.5:n.1573G>A
ENST00000601008.1:c.242-1183G>A	ENSP00000471384.1:n.242-1183G>A
ENST00000602229.1:c.61G>A
NM_000064.3:c.4614G>A	NP_000055.2:p.Glu1538=
NM_000064.4:c.4614G>A MANE Select	NP_000055.2:p.Glu1538=