Canonical Allele Identifier: CA403620165

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686280T>A (hg19) ; chr19:g.6686269T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686269T>A , CM000681.2:g.6686269T>A	GRCh38
NC_000019.9:g.6686280T>A , CM000681.1:g.6686280T>A	GRCh37
NC_000019.8:g.6637280T>A	NCBI36
NG_009557.1:g.39383A>T , LRG_27:g.39383A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2013A>T
ENST00000695652.1:c.3542A>T	ENSP00000512083.1:p.Asp1181Val
ENST00000695653.1:c.1574A>T	ENSP00000512084.1:p.Asp525Val
ENST00000695654.1:c.2690A>T	ENSP00000512085.1:p.Asp897Val
ENST00000695655.1:c.2606A>T	ENSP00000512086.1:n.2606A>T
ENST00000695692.1:n.3029A>T
ENST00000245907.11:c.3665A>T MANE Select	ENSP00000245907.4:p.Asp1222Val
ENST00000245907.10:c.3665A>T	ENSP00000245907.4:p.Asp1222Val
ENST00000596238.1:n.108A>T
ENST00000601008.1:c.241+477A>T	ENSP00000471384.1:n.241+477A>T
NM_000064.3:c.3665A>T	NP_000055.2:p.Asp1222Val
NM_000064.4:c.3665A>T MANE Select	NP_000055.2:p.Asp1222Val