Canonical Allele Identifier: CA505123662

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686156A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686145A>C , CM000681.2:g.6686145A>C	GRCh38
NC_000019.9:g.6686156A>C , CM000681.1:g.6686156A>C	GRCh37
NC_000019.8:g.6637156A>C	NCBI36
NG_009557.1:g.39507T>G , LRG_27:g.39507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2137T>G
ENST00000695652.1:c.3666T>G	ENSP00000512083.1:p.Gly1222=
ENST00000695653.1:c.1698T>G	ENSP00000512084.1:p.Gly566=
ENST00000695654.1:c.2814T>G	ENSP00000512085.1:p.Gly938=
ENST00000695655.1:c.2730T>G	ENSP00000512086.1:n.2730T>G
ENST00000695692.1:n.3153T>G
ENST00000245907.11:c.3789T>G MANE Select	ENSP00000245907.4:p.Gly1263=
ENST00000245907.10:c.3789T>G	ENSP00000245907.4:p.Gly1263=
ENST00000596238.1:n.232T>G
ENST00000601008.1:c.241+601T>G	ENSP00000471384.1:n.241+601T>G
NM_000064.3:c.3789T>G	NP_000055.2:p.Gly1263=
NM_000064.4:c.3789T>G MANE Select	NP_000055.2:p.Gly1263=