Canonical Allele Identifier: CA2577765441
Gene: MIOX HGNC NCBI

Linked Data

gnomAD v4: 22-50489928-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489928G>A , CM000684.2:g.50489928G>A GRCh38
NC_000022.10:g.50928357G>A , CM000684.1:g.50928357G>A GRCh37
NC_000022.9:g.49275223G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*72G>A MANE Select ENSP00000216075.6:n.*72G>A
ENST00000216075.10:c.*72G>A ENSP00000216075.6:n.*72G>A
ENST00000395732.7:c.*103G>A ENSP00000379081.3:n.*103G>A
ENST00000395733.7:c.*103G>A ENSP00000379082.3:n.*103G>A
ENST00000451761.1:c.870G>A ENSP00000409894.1:n.870G>A
NM_017584.5:c.*72G>A NP_060054.4:n.*72G>A
XM_005261925.3:c.*72G>A XP_005261982.1:n.*72G>A
XR_244455.2:n.3426G>A
XM_005261925.4:c.*72G>A XP_005261982.1:n.*72G>A
NM_017584.6:c.*72G>A MANE Select NP_060054.4:n.*72G>A
Search 100 bp 5'
Search 100 bp 3'