Canonical Allele Identifier: CA9129002

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697470G>C , CM000681.2:g.6697470G>C	GRCh38
NC_000019.9:g.6697481G>C , CM000681.1:g.6697481G>C	GRCh37
NC_000019.8:g.6648481G>C	NCBI36
NG_009557.1:g.28182C>G , LRG_27:g.28182C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000064.4:c.2670C>G MANE Select	NP_000055.2:p.Pro890=
ENST00000245907.11:c.2670C>G MANE Select	ENSP00000245907.4:p.Pro890=
NM_000064.3:c.2670C>G	NP_000055.2:p.Pro890=
ENST00000245907.10:c.2670C>G	ENSP00000245907.4:p.Pro890=
ENST00000594005.1:n.246C>G
ENST00000695651.1:n.1018C>G
ENST00000695652.1:c.2547C>G	ENSP00000512083.1:p.Pro849=
ENST00000695653.1:c.579C>G	ENSP00000512084.1:p.Pro193=
ENST00000695654.1:c.1794C>G	ENSP00000512085.1:p.Pro598=
ENST00000695655.1:c.1611C>G	ENSP00000512086.1:n.1611C>G
ENST00000695692.1:n.2034C>G