Canonical Allele Identifier: CA2657564232
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489930A>G , CM000684.2:g.50489930A>G GRCh38
NC_000022.10:g.50928359A>G , CM000684.1:g.50928359A>G GRCh37
NC_000022.9:g.49275225A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*74A>G MANE Select ENSP00000216075.6:n.*74A>G
ENST00000216075.10:c.*74A>G ENSP00000216075.6:n.*74A>G
ENST00000395732.7:c.*105A>G ENSP00000379081.3:n.*105A>G
ENST00000395733.7:c.*105A>G ENSP00000379082.3:n.*105A>G
ENST00000451761.1:c.872A>G ENSP00000409894.1:n.872A>G
NM_017584.5:c.*74A>G NP_060054.4:n.*74A>G
XM_005261925.3:c.*74A>G XP_005261982.1:n.*74A>G
XR_244455.2:n.3428A>G
XM_005261925.4:c.*74A>G XP_005261982.1:n.*74A>G
NM_017584.6:c.*74A>G MANE Select NP_060054.4:n.*74A>G