Canonical Allele Identifier: CA505124809

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709806C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709795C>T , CM000681.2:g.6709795C>T	GRCh38
NC_000019.9:g.6709806C>T , CM000681.1:g.6709806C>T	GRCh37
NC_000019.8:g.6660806C>T	NCBI36
NG_009557.1:g.15857G>A , LRG_27:g.15857G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1611G>A	ENSP00000512083.1:p.Gly537=
ENST00000695654.1:c.858G>A	ENSP00000512085.1:p.Gly286=
ENST00000695655.1:c.675G>A	ENSP00000512086.1:n.675G>A
ENST00000695692.1:n.1098G>A
ENST00000245907.11:c.1734G>A MANE Select	ENSP00000245907.4:p.Gly578=
ENST00000245907.10:c.1734G>A	ENSP00000245907.4:p.Gly578=
ENST00000600763.1:n.367G>A
NM_000064.3:c.1734G>A	NP_000055.2:p.Gly578=
NM_000064.4:c.1734G>A MANE Select	NP_000055.2:p.Gly578=