Canonical Allele Identifier: CA3054019532
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662891_26662892insCTT , CM000684.2:g.26662891_26662892insCTT GRCh38
NC_000022.10:g.27058855_27058856insCTT , CM000684.1:g.27058855_27058856insCTT GRCh37
NC_000022.9:g.25388855_25388856insCTT NCBI36
NG_016621.2:g.10410_10411insCTT

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-425_174-424insCTT
NR_033319.2:n.174-425_174-424insCTT
NR_033320.2:n.174-425_174-424insCTT
NR_033321.2:n.174-425_174-424insCTT