Canonical Allele Identifier: CA403619482

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686169T>G (hg19) ; chr19:g.6686158T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686158T>G , CM000681.2:g.6686158T>G	GRCh38
NC_000019.9:g.6686169T>G , CM000681.1:g.6686169T>G	GRCh37
NC_000019.8:g.6637169T>G	NCBI36
NG_009557.1:g.39494A>C , LRG_27:g.39494A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2124A>C
ENST00000695652.1:c.3653A>C	ENSP00000512083.1:p.Gln1218Pro
ENST00000695653.1:c.1685A>C	ENSP00000512084.1:p.Gln562Pro
ENST00000695654.1:c.2801A>C	ENSP00000512085.1:p.Gln934Pro
ENST00000695655.1:c.2717A>C	ENSP00000512086.1:n.2717A>C
ENST00000695692.1:n.3140A>C
ENST00000245907.11:c.3776A>C MANE Select	ENSP00000245907.4:p.Gln1259Pro
ENST00000245907.10:c.3776A>C	ENSP00000245907.4:p.Gln1259Pro
ENST00000596238.1:n.219A>C
ENST00000601008.1:c.241+588A>C	ENSP00000471384.1:n.241+588A>C
NM_000064.3:c.3776A>C	NP_000055.2:p.Gln1259Pro
NM_000064.4:c.3776A>C MANE Select	NP_000055.2:p.Gln1259Pro