Canonical Allele Identifier: CA403633748

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697677T>G (hg19) ; chr19:g.6697666T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697666T>G , CM000681.2:g.6697666T>G	GRCh38
NC_000019.9:g.6697677T>G , CM000681.1:g.6697677T>G	GRCh37
NC_000019.8:g.6648677T>G	NCBI36
NG_009557.1:g.27986A>C , LRG_27:g.27986A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.917A>C
ENST00000695652.1:c.2446A>C	ENSP00000512083.1:p.Asn816His
ENST00000695653.1:c.478A>C	ENSP00000512084.1:p.Asn160His
ENST00000695654.1:c.1693A>C	ENSP00000512085.1:p.Asn565His
ENST00000695655.1:c.1510A>C	ENSP00000512086.1:n.1510A>C
ENST00000695692.1:n.1933A>C
ENST00000245907.11:c.2569A>C MANE Select	ENSP00000245907.4:p.Asn857His
ENST00000245907.10:c.2569A>C	ENSP00000245907.4:p.Asn857His
ENST00000594005.1:n.50A>C
ENST00000602053.1:n.617A>C
NM_000064.3:c.2569A>C	NP_000055.2:p.Asn857His
NM_000064.4:c.2569A>C MANE Select	NP_000055.2:p.Asn857His