Canonical Allele Identifier: CA14963152
Gene: MIOX HGNC NCBI

Linked Data

dbSNP Id: rs2232873

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50486669G>A , CM000684.2:g.50486669G>A GRCh38
NC_000022.10:g.50925098G>A , CM000684.1:g.50925098G>A GRCh37
NC_000022.9:g.49271964G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011530705.1:c.-64-165G>A XP_011529007.1:n.-64-165G>A
XR_244455.2:n.2401-165G>A
XM_011530705.2:c.-64-165G>A XP_011529007.1:n.-64-165G>A