Canonical Allele Identifier: CA403634008

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697752C>G (hg19) ; chr19:g.6697741C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697741C>G , CM000681.2:g.6697741C>G	GRCh38
NC_000019.9:g.6697752C>G , CM000681.1:g.6697752C>G	GRCh37
NC_000019.8:g.6648752C>G	NCBI36
NG_009557.1:g.27911G>C , LRG_27:g.27911G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.842G>C
ENST00000695652.1:c.2371G>C	ENSP00000512083.1:p.Asp791His
ENST00000695653.1:c.403G>C	ENSP00000512084.1:p.Asp135His
ENST00000695654.1:c.1618G>C	ENSP00000512085.1:p.Asp540His
ENST00000695655.1:c.1435G>C	ENSP00000512086.1:n.1435G>C
ENST00000695692.1:n.1858G>C
ENST00000245907.11:c.2494G>C MANE Select	ENSP00000245907.4:p.Asp832His
ENST00000245907.10:c.2494G>C	ENSP00000245907.4:p.Asp832His
ENST00000602053.1:n.542G>C
NM_000064.3:c.2494G>C	NP_000055.2:p.Asp832His
NM_000064.4:c.2494G>C MANE Select	NP_000055.2:p.Asp832His