Canonical Allele Identifier: CA10670823
Gene: UQCRH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11588062

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46314092C>T , CM000663.2:g.46314092C>T GRCh38
NC_000001.9:g.46552351C>T NCBI36
NC_000001.10:g.46779764C>T , CM000663.1:g.46779764C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000311672.9:c.244-2460C>T ENSP00000309565.5:p.=
ENST00000460947.1:n.397-2460C>T
ENST00000489056.5:c.*83-2460C>T ENSP00000484857.1:p.=
ENST00000496387.5:c.*83-2460C>T ENSP00000477826.1:p.=
NM_001297565.1:c.226-2460C>T VV NP_001284494.1:p.=
NM_001297566.1:c.217-2460C>T VV NP_001284495.1:p.=
NM_006004.3:c.244-2460C>T VV NP_005995.2:p.=