Canonical Allele Identifier: CA2399297452
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662975T= , CM000684.2:g.26662975T= GRCh38
NC_000022.10:g.27058939T= , CM000684.1:g.27058939T= GRCh37
NC_000022.9:g.25388939T= NCBI36
NG_016621.2:g.10494T=

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-341T=
NR_033319.2:n.174-341T=
NR_033320.2:n.174-341T=
NR_033321.2:n.174-341T=