Canonical Allele Identifier: CA403612841

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679487A>C (hg19) ; chr19:g.6679476A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679476A>C , CM000681.2:g.6679476A>C	GRCh38
NC_000019.9:g.6679487A>C , CM000681.1:g.6679487A>C	GRCh37
NC_000019.8:g.6630487A>C	NCBI36
NG_009557.1:g.46176T>G , LRG_27:g.46176T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2825T>G
ENST00000695653.1:c.2386T>G	ENSP00000512084.1:p.Tyr796Asp
ENST00000695654.1:c.3502T>G	ENSP00000512085.1:p.Tyr1168Asp
ENST00000695689.1:c.448T>G	ENSP00000512101.1:n.448T>G
ENST00000695690.1:n.1542T>G
ENST00000695691.1:n.1338T>G
ENST00000245907.11:c.4477T>G MANE Select	ENSP00000245907.4:p.Tyr1493Asp
ENST00000245907.10:c.4477T>G	ENSP00000245907.4:p.Tyr1493Asp
ENST00000599668.1:n.72T>G
ENST00000599899.5:n.1436T>G
ENST00000601008.1:c.242-1518T>G	ENSP00000471384.1:n.242-1518T>G
NM_000064.3:c.4477T>G	NP_000055.2:p.Tyr1493Asp
NM_000064.4:c.4477T>G MANE Select	NP_000055.2:p.Tyr1493Asp