Canonical Allele Identifier: CA2657564211
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489917C>T , CM000684.2:g.50489917C>T GRCh38
NC_000022.10:g.50928346C>T , CM000684.1:g.50928346C>T GRCh37
NC_000022.9:g.49275212C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*61C>T MANE Select ENSP00000216075.6:n.*61C>T
ENST00000216075.10:c.*61C>T ENSP00000216075.6:n.*61C>T
ENST00000395732.7:c.*92C>T ENSP00000379081.3:n.*92C>T
ENST00000395733.7:c.*92C>T ENSP00000379082.3:n.*92C>T
ENST00000451761.1:c.859C>T ENSP00000409894.1:n.859C>T
NM_017584.5:c.*61C>T NP_060054.4:n.*61C>T
XM_005261925.3:c.*61C>T XP_005261982.1:n.*61C>T
XR_244455.2:n.3415C>T
XM_005261925.4:c.*61C>T XP_005261982.1:n.*61C>T
NM_017584.6:c.*61C>T MANE Select NP_060054.4:n.*61C>T