Canonical Allele Identifier: CA736253787

Gene: UQCRH

Linked Data

• dbSNP Id: rs965417373
• MyVariant Identifiers: chr1:g.46779707T>C (hg19) ; chr1:g.46314035T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46314035T>C , CM000663.2:g.46314035T>C	GRCh38
NC_000001.10:g.46779707T>C , CM000663.1:g.46779707T>C	GRCh37
NC_000001.9:g.46552294T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000311672.10:c.244-2517T>C MANE Select	ENSP00000309565.5:n.244-2517T>C
ENST00000311672.9:c.244-2517T>C	ENSP00000309565.5:n.244-2517T>C
ENST00000460947.1:n.397-2517T>C
ENST00000489056.5:c.*83-2517T>C	ENSP00000484857.1:n.*83-2517T>C
ENST00000496387.5:c.*83-2517T>C	ENSP00000477826.1:n.*83-2517T>C
NM_001297565.1:c.226-2517T>C	NP_001284494.1:n.226-2517T>C
NM_001297566.1:c.217-2517T>C	NP_001284495.1:n.217-2517T>C
NM_006004.3:c.244-2517T>C	NP_005995.2:n.244-2517T>C
NM_006004.4:c.244-2517T>C MANE Select	NP_005995.2:n.244-2517T>C
NM_001297565.2:c.226-2517T>C	NP_001284494.1:n.226-2517T>C
NM_001297566.2:c.217-2517T>C	NP_001284495.1:n.217-2517T>C