Canonical Allele Identifier: CA322664878
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs549000250
gnomAD v3: 22-26662665-G-A
gnomAD v4: 22-26662665-G-A
COSMIC: COSN20977884
MyVariant Identifiers: chr22:g.27058629G>A (hg19) chr22:g.26662665G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662665G>A , CM000684.2:g.26662665G>A GRCh38
NC_000022.10:g.27058629G>A , CM000684.1:g.27058629G>A GRCh37
NC_000022.9:g.25388629G>A NCBI36
NG_016621.2:g.10184G>A

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-651G>A
NR_033319.2:n.174-651G>A
NR_033320.2:n.174-651G>A
NR_033321.2:n.174-651G>A
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