Canonical Allele Identifier: CA2399297373
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662759_26662760delinsGA , CM000684.2:g.26662759_26662760delinsGA GRCh38
NC_000022.10:g.27058723_27058724delinsGA , CM000684.1:g.27058723_27058724delinsGA GRCh37
NC_000022.9:g.25388723_25388724delinsGA NCBI36
NG_016621.2:g.10278_10279delinsGA

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-557_174-556delinsGA
NR_033319.2:n.174-557_174-556delinsGA
NR_033320.2:n.174-557_174-556delinsGA
NR_033321.2:n.174-557_174-556delinsGA