Canonical Allele Identifier: CA403633196

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697505G>T (hg19) ; chr19:g.6697494G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697494G>T , CM000681.2:g.6697494G>T	GRCh38
NC_000019.9:g.6697505G>T , CM000681.1:g.6697505G>T	GRCh37
NC_000019.8:g.6648505G>T	NCBI36
NG_009557.1:g.28158C>A , LRG_27:g.28158C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.994C>A
ENST00000695652.1:c.2523C>A	ENSP00000512083.1:p.His841Gln
ENST00000695653.1:c.555C>A	ENSP00000512084.1:p.His185Gln
ENST00000695654.1:c.1770C>A	ENSP00000512085.1:p.His590Gln
ENST00000695655.1:c.1587C>A	ENSP00000512086.1:n.1587C>A
ENST00000695692.1:n.2010C>A
ENST00000245907.11:c.2646C>A MANE Select	ENSP00000245907.4:p.His882Gln
ENST00000245907.10:c.2646C>A	ENSP00000245907.4:p.His882Gln
ENST00000594005.1:n.222C>A
NM_000064.3:c.2646C>A	NP_000055.2:p.His882Gln
NM_000064.4:c.2646C>A MANE Select	NP_000055.2:p.His882Gln