Canonical Allele Identifier: CA403645085

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6718288C>G (hg19) ; chr19:g.6718277C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718277C>G , CM000681.2:g.6718277C>G	GRCh38
NC_000019.9:g.6718288C>G , CM000681.1:g.6718288C>G	GRCh37
NC_000019.8:g.6669288C>G	NCBI36
NG_009557.1:g.7375G>C , LRG_27:g.7375G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000594936.2:n.464G>C
ENST00000695652.1:c.280G>C	ENSP00000512083.1:p.Asp94His
ENST00000695693.1:c.403G>C	ENSP00000512104.1:p.Asp135His
ENST00000245907.11:c.403G>C MANE Select	ENSP00000245907.4:p.Asp135His
ENST00000245907.10:c.403G>C	ENSP00000245907.4:p.Asp135His
ENST00000594936.1:n.464G>C
ENST00000600744.1:c.280G>C	ENSP00000472044.1:p.Asp94His
NM_000064.3:c.403G>C	NP_000055.2:p.Asp135His
NM_000064.4:c.403G>C MANE Select	NP_000055.2:p.Asp135His