Canonical Allele Identifier: CA403634071

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697767G>T (hg19) ; chr19:g.6697756G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697756G>T , CM000681.2:g.6697756G>T	GRCh38
NC_000019.9:g.6697767G>T , CM000681.1:g.6697767G>T	GRCh37
NC_000019.8:g.6648767G>T	NCBI36
NG_009557.1:g.27896C>A , LRG_27:g.27896C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.827C>A
ENST00000695652.1:c.2356C>A	ENSP00000512083.1:p.Gln786Lys
ENST00000695653.1:c.388C>A	ENSP00000512084.1:p.Gln130Lys
ENST00000695654.1:c.1603C>A	ENSP00000512085.1:p.Gln535Lys
ENST00000695655.1:c.1420C>A	ENSP00000512086.1:n.1420C>A
ENST00000695692.1:n.1843C>A
ENST00000245907.11:c.2479C>A MANE Select	ENSP00000245907.4:p.Gln827Lys
ENST00000245907.10:c.2479C>A	ENSP00000245907.4:p.Gln827Lys
ENST00000602053.1:n.527C>A
NM_000064.3:c.2479C>A	NP_000055.2:p.Gln827Lys
NM_000064.4:c.2479C>A MANE Select	NP_000055.2:p.Gln827Lys