Canonical Allele Identifier: CA412150538
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489822T>G , CM000684.2:g.50489822T>G GRCh38
NC_000022.10:g.50928251T>G , CM000684.1:g.50928251T>G GRCh37
NC_000022.9:g.49275117T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.824T>G MANE Select ENSP00000216075.6:p.Ile275Ser
ENST00000216075.10:c.824T>G ENSP00000216075.6:p.Ile275Ser
ENST00000395732.7:c.810T>G ENSP00000379081.3:p.His270Gln
ENST00000395733.7:c.693T>G ENSP00000379082.3:p.His231Gln
ENST00000451761.1:c.764T>G ENSP00000409894.1:p.Ile255Ser
NM_017584.5:c.824T>G NP_060054.4:p.Ile275Ser
XM_005261925.3:c.686T>G XP_005261982.1:p.Ile229Ser
XR_244455.2:n.3320T>G
XM_005261925.4:c.686T>G XP_005261982.1:p.Ile229Ser
NM_017584.6:c.824T>G MANE Select NP_060054.4:p.Ile275Ser