Canonical Allele Identifier: CA752042629
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1244493050
gnomAD v3: 22-26662726-A-G
gnomAD v4: 22-26662726-A-G
MyVariant Identifiers: chr22:g.27058690A>G (hg19) chr22:g.26662726A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662726A>G , CM000684.2:g.26662726A>G GRCh38
NC_000022.10:g.27058690A>G , CM000684.1:g.27058690A>G GRCh37
NC_000022.9:g.25388690A>G NCBI36
NG_016621.2:g.10245A>G

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-590A>G
NR_033319.2:n.174-590A>G
NR_033320.2:n.174-590A>G
NR_033321.2:n.174-590A>G
Search 100 bp 5'
Search 100 bp 3'