Canonical Allele Identifier: CA640044416
Gene: MIOX HGNC NCBI

Linked Data

dbSNP Id: rs1177933210
gnomAD v2: 22-50928355-G-C
gnomAD v4: 22-50489926-G-C
MyVariant Identifiers: chr22:g.50928355G>C (hg19) chr22:g.50489926G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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