Canonical Allele Identifier: CA403634032

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697758A>T (hg19) ; chr19:g.6697747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697747A>T , CM000681.2:g.6697747A>T	GRCh38
NC_000019.9:g.6697758A>T , CM000681.1:g.6697758A>T	GRCh37
NC_000019.8:g.6648758A>T	NCBI36
NG_009557.1:g.27905T>A , LRG_27:g.27905T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.836T>A
ENST00000695652.1:c.2365T>A	ENSP00000512083.1:p.Phe789Ile
ENST00000695653.1:c.397T>A	ENSP00000512084.1:p.Phe133Ile
ENST00000695654.1:c.1612T>A	ENSP00000512085.1:p.Phe538Ile
ENST00000695655.1:c.1429T>A	ENSP00000512086.1:n.1429T>A
ENST00000695692.1:n.1852T>A
ENST00000245907.11:c.2488T>A MANE Select	ENSP00000245907.4:p.Phe830Ile
ENST00000245907.10:c.2488T>A	ENSP00000245907.4:p.Phe830Ile
ENST00000602053.1:n.536T>A
NM_000064.3:c.2488T>A	NP_000055.2:p.Phe830Ile
NM_000064.4:c.2488T>A MANE Select	NP_000055.2:p.Phe830Ile