Canonical Allele Identifier: CA412150484
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489814G>T , CM000684.2:g.50489814G>T GRCh38
NC_000022.10:g.50928243G>T , CM000684.1:g.50928243G>T GRCh37
NC_000022.9:g.49275109G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.816G>T MANE Select ENSP00000216075.6:p.Gln272His
ENST00000216075.10:c.816G>T ENSP00000216075.6:p.Gln272His
ENST00000395732.7:c.802G>T ENSP00000379081.3:p.Gly268Trp
ENST00000395733.7:c.685G>T ENSP00000379082.3:p.Gly229Trp
ENST00000451761.1:c.756G>T ENSP00000409894.1:p.Gln252His
NM_017584.5:c.816G>T NP_060054.4:p.Gln272His
XM_005261925.3:c.678G>T XP_005261982.1:p.Gln226His
XR_244455.2:n.3312G>T
XM_005261925.4:c.678G>T XP_005261982.1:p.Gln226His
NM_017584.6:c.816G>T MANE Select NP_060054.4:p.Gln272His