Canonical Allele Identifier: CA322664893
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs181021902

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662802G>A , CM000684.2:g.26662802G>A GRCh38
NC_000022.10:g.27058766G>A , CM000684.1:g.27058766G>A GRCh37
NC_000022.9:g.25388766G>A NCBI36
NG_016621.2:g.10321G>A

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-514G>A
NR_033319.2:n.174-514G>A
NR_033320.2:n.174-514G>A
NR_033321.2:n.174-514G>A