Canonical Allele Identifier: CA505192475

Gene: C3

Linked Data

• gnomAD v4: 19-6697693-G-T
• MyVariant Identifiers: chr19:g.6697704G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697693G>T , CM000681.2:g.6697693G>T	GRCh38
NC_000019.9:g.6697704G>T , CM000681.1:g.6697704G>T	GRCh37
NC_000019.8:g.6648704G>T	NCBI36
NG_009557.1:g.27959C>A , LRG_27:g.27959C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.890C>A
ENST00000695652.1:c.2419C>A	ENSP00000512083.1:p.Arg807=
ENST00000695653.1:c.451C>A	ENSP00000512084.1:p.Arg151=
ENST00000695654.1:c.1666C>A	ENSP00000512085.1:p.Arg556=
ENST00000695655.1:c.1483C>A	ENSP00000512086.1:n.1483C>A
ENST00000695692.1:n.1906C>A
ENST00000245907.11:c.2542C>A MANE Select	ENSP00000245907.4:p.Arg848=
ENST00000245907.10:c.2542C>A	ENSP00000245907.4:p.Arg848=
ENST00000594005.1:n.23C>A
ENST00000602053.1:n.590C>A
NM_000064.3:c.2542C>A	NP_000055.2:p.Arg848=
NM_000064.4:c.2542C>A MANE Select	NP_000055.2:p.Arg848=