Canonical Allele Identifier: CA403633908

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697710C>T (hg19) ; chr19:g.6697699C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697699C>T , CM000681.2:g.6697699C>T	GRCh38
NC_000019.9:g.6697710C>T , CM000681.1:g.6697710C>T	GRCh37
NC_000019.8:g.6648710C>T	NCBI36
NG_009557.1:g.27953G>A , LRG_27:g.27953G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.884G>A
ENST00000695652.1:c.2413G>A	ENSP00000512083.1:p.Glu805Lys
ENST00000695653.1:c.445G>A	ENSP00000512084.1:p.Glu149Lys
ENST00000695654.1:c.1660G>A	ENSP00000512085.1:p.Glu554Lys
ENST00000695655.1:c.1477G>A	ENSP00000512086.1:n.1477G>A
ENST00000695692.1:n.1900G>A
ENST00000245907.11:c.2536G>A MANE Select	ENSP00000245907.4:p.Glu846Lys
ENST00000245907.10:c.2536G>A	ENSP00000245907.4:p.Glu846Lys
ENST00000594005.1:n.17G>A
ENST00000602053.1:n.584G>A
NM_000064.3:c.2536G>A	NP_000055.2:p.Glu846Lys
NM_000064.4:c.2536G>A MANE Select	NP_000055.2:p.Glu846Lys