Canonical Allele Identifier: CA638869676
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1269405806
gnomAD v2: 22-27058674-C-T
gnomAD v3: 22-26662710-C-T
gnomAD v4: 22-26662710-C-T
MyVariant Identifiers: chr22:g.27058674C>T (hg19) chr22:g.26662710C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662710C>T , CM000684.2:g.26662710C>T GRCh38
NC_000022.10:g.27058674C>T , CM000684.1:g.27058674C>T GRCh37
NC_000022.9:g.25388674C>T NCBI36
NG_016621.2:g.10229C>T

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-606C>T
NR_033319.2:n.174-606C>T
NR_033320.2:n.174-606C>T
NR_033321.2:n.174-606C>T
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