Canonical Allele Identifier: CA403633838

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697694A>T (hg19) ; chr19:g.6697683A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697683A>T , CM000681.2:g.6697683A>T	GRCh38
NC_000019.9:g.6697694A>T , CM000681.1:g.6697694A>T	GRCh37
NC_000019.8:g.6648694A>T	NCBI36
NG_009557.1:g.27969T>A , LRG_27:g.27969T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.900T>A
ENST00000695652.1:c.2429T>A	ENSP00000512083.1:p.Leu810His
ENST00000695653.1:c.461T>A	ENSP00000512084.1:p.Leu154His
ENST00000695654.1:c.1676T>A	ENSP00000512085.1:p.Leu559His
ENST00000695655.1:c.1493T>A	ENSP00000512086.1:n.1493T>A
ENST00000695692.1:n.1916T>A
ENST00000245907.11:c.2552T>A MANE Select	ENSP00000245907.4:p.Leu851His
ENST00000245907.10:c.2552T>A	ENSP00000245907.4:p.Leu851His
ENST00000594005.1:n.33T>A
ENST00000602053.1:n.600T>A
NM_000064.3:c.2552T>A	NP_000055.2:p.Leu851His
NM_000064.4:c.2552T>A MANE Select	NP_000055.2:p.Leu851His