Canonical Allele Identifier: CA2410885407
Gene: MIOX HGNC NCBI

Linked Data

dbSNP Id: rs1177933210
gnomAD v4: 22-50489926-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489926G>A , CM000684.2:g.50489926G>A GRCh38
NC_000022.10:g.50928355G>A , CM000684.1:g.50928355G>A GRCh37
NC_000022.9:g.49275221G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*70G>A MANE Select ENSP00000216075.6:n.*70G>A
ENST00000216075.10:c.*70G>A ENSP00000216075.6:n.*70G>A
ENST00000395732.7:c.*101G>A ENSP00000379081.3:n.*101G>A
ENST00000395733.7:c.*101G>A ENSP00000379082.3:n.*101G>A
ENST00000451761.1:c.868G>A ENSP00000409894.1:n.868G>A
NM_017584.5:c.*70G>A NP_060054.4:n.*70G>A
XM_005261925.3:c.*70G>A XP_005261982.1:n.*70G>A
XR_244455.2:n.3424G>A
XM_005261925.4:c.*70G>A XP_005261982.1:n.*70G>A
NM_017584.6:c.*70G>A MANE Select NP_060054.4:n.*70G>A
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