Canonical Allele Identifier: CA403633699

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697670T>C (hg19) ; chr19:g.6697659T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697659T>C , CM000681.2:g.6697659T>C	GRCh38
NC_000019.9:g.6697670T>C , CM000681.1:g.6697670T>C	GRCh37
NC_000019.8:g.6648670T>C	NCBI36
NG_009557.1:g.27993A>G , LRG_27:g.27993A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.924A>G
ENST00000695652.1:c.2453A>G	ENSP00000512083.1:p.Glu818Gly
ENST00000695653.1:c.485A>G	ENSP00000512084.1:p.Glu162Gly
ENST00000695654.1:c.1700A>G	ENSP00000512085.1:p.Glu567Gly
ENST00000695655.1:c.1517A>G	ENSP00000512086.1:n.1517A>G
ENST00000695692.1:n.1940A>G
ENST00000245907.11:c.2576A>G MANE Select	ENSP00000245907.4:p.Glu859Gly
ENST00000245907.10:c.2576A>G	ENSP00000245907.4:p.Glu859Gly
ENST00000594005.1:n.57A>G
NM_000064.3:c.2576A>G	NP_000055.2:p.Glu859Gly
NM_000064.4:c.2576A>G MANE Select	NP_000055.2:p.Glu859Gly