Canonical Allele Identifier: CA403632683

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697395T>C (hg19) ; chr19:g.6697384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697384T>C , CM000681.2:g.6697384T>C	GRCh38
NC_000019.9:g.6697395T>C , CM000681.1:g.6697395T>C	GRCh37
NC_000019.8:g.6648395T>C	NCBI36
NG_009557.1:g.28268A>G , LRG_27:g.28268A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1104A>G
ENST00000695652.1:c.2633A>G	ENSP00000512083.1:p.His878Arg
ENST00000695653.1:c.665A>G	ENSP00000512084.1:p.His222Arg
ENST00000695654.1:c.1880A>G	ENSP00000512085.1:p.His627Arg
ENST00000695655.1:c.1697A>G	ENSP00000512086.1:n.1697A>G
ENST00000695692.1:n.2120A>G
ENST00000245907.11:c.2756A>G MANE Select	ENSP00000245907.4:p.His919Arg
ENST00000245907.10:c.2756A>G	ENSP00000245907.4:p.His919Arg
ENST00000594005.1:n.332A>G
NM_000064.3:c.2756A>G	NP_000055.2:p.His919Arg
NM_000064.4:c.2756A>G MANE Select	NP_000055.2:p.His919Arg