Canonical Allele Identifier: CA2657564216
Gene: MIOX HGNC NCBI

Linked Data

gnomAD v4: 22-50489921-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489921G>A , CM000684.2:g.50489921G>A GRCh38
NC_000022.10:g.50928350G>A , CM000684.1:g.50928350G>A GRCh37
NC_000022.9:g.49275216G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*65G>A MANE Select ENSP00000216075.6:n.*65G>A
ENST00000216075.10:c.*65G>A ENSP00000216075.6:n.*65G>A
ENST00000395732.7:c.*96G>A ENSP00000379081.3:n.*96G>A
ENST00000395733.7:c.*96G>A ENSP00000379082.3:n.*96G>A
ENST00000451761.1:c.863G>A ENSP00000409894.1:n.863G>A
NM_017584.5:c.*65G>A NP_060054.4:n.*65G>A
XM_005261925.3:c.*65G>A XP_005261982.1:n.*65G>A
XR_244455.2:n.3419G>A
XM_005261925.4:c.*65G>A XP_005261982.1:n.*65G>A
NM_017584.6:c.*65G>A MANE Select NP_060054.4:n.*65G>A
Search 100 bp 5'
Search 100 bp 3'