Canonical Allele Identifier: CA322664905
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1012664930
gnomAD v3: 22-26662973-G-T
gnomAD v4: 22-26662973-G-T
MyVariant Identifiers: chr22:g.27058937G>T (hg19) chr22:g.26662973G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662973G>T , CM000684.2:g.26662973G>T GRCh38
NC_000022.10:g.27058937G>T , CM000684.1:g.27058937G>T GRCh37
NC_000022.9:g.25388937G>T NCBI36
NG_016621.2:g.10492G>T

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-343G>T
NR_033319.2:n.174-343G>T
NR_033320.2:n.174-343G>T
NR_033321.2:n.174-343G>T
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