Canonical Allele Identifier: CA2818611684
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662735T>A , CM000684.2:g.26662735T>A GRCh38
NC_000022.10:g.27058699T>A , CM000684.1:g.27058699T>A GRCh37
NC_000022.9:g.25388699T>A NCBI36
NG_016621.2:g.10254T>A

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-581T>A
NR_033319.2:n.174-581T>A
NR_033320.2:n.174-581T>A
NR_033321.2:n.174-581T>A