Canonical Allele Identifier: CA2589650418
Gene: MIAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662907_26662909dup , CM000684.2:g.26662907_26662909dup GRCh38
NC_000022.10:g.27058871_27058873dup , CM000684.1:g.27058871_27058873dup GRCh37
NC_000022.9:g.25388871_25388873dup NCBI36
NG_016621.2:g.10426_10428dup

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-409_174-407dup
NR_033319.2:n.174-409_174-407dup
NR_033320.2:n.174-409_174-407dup
NR_033321.2:n.174-409_174-407dup