Canonical Allele Identifier: CA505192473

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697702T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697691T>G , CM000681.2:g.6697691T>G	GRCh38
NC_000019.9:g.6697702T>G , CM000681.1:g.6697702T>G	GRCh37
NC_000019.8:g.6648702T>G	NCBI36
NG_009557.1:g.27961A>C , LRG_27:g.27961A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.892A>C
ENST00000695652.1:c.2421A>C	ENSP00000512083.1:p.Arg807=
ENST00000695653.1:c.453A>C	ENSP00000512084.1:p.Arg151=
ENST00000695654.1:c.1668A>C	ENSP00000512085.1:p.Arg556=
ENST00000695655.1:c.1485A>C	ENSP00000512086.1:n.1485A>C
ENST00000695692.1:n.1908A>C
ENST00000245907.11:c.2544A>C MANE Select	ENSP00000245907.4:p.Arg848=
ENST00000245907.10:c.2544A>C	ENSP00000245907.4:p.Arg848=
ENST00000594005.1:n.25A>C
ENST00000602053.1:n.592A>C
NM_000064.3:c.2544A>C	NP_000055.2:p.Arg848=
NM_000064.4:c.2544A>C MANE Select	NP_000055.2:p.Arg848=