Canonical Allele Identifier: CA322664909
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1002676018
gnomAD v3: 22-26662995-G-A
gnomAD v4: 22-26662995-G-A
MyVariant Identifiers: chr22:g.27058959G>A (hg19) chr22:g.26662995G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662995G>A , CM000684.2:g.26662995G>A GRCh38
NC_000022.10:g.27058959G>A , CM000684.1:g.27058959G>A GRCh37
NC_000022.9:g.25388959G>A NCBI36
NG_016621.2:g.10514G>A

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-321G>A
NR_033319.2:n.174-321G>A
NR_033320.2:n.174-321G>A
NR_033321.2:n.174-321G>A
Search 100 bp 5'
Search 100 bp 3'