Canonical Allele Identifier: CA322664904
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1005092523
MyVariant Identifiers: chr22:g.27058926T>A (hg19) chr22:g.26662962T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662962T>A , CM000684.2:g.26662962T>A GRCh38
NC_000022.10:g.27058926T>A , CM000684.1:g.27058926T>A GRCh37
NC_000022.9:g.25388926T>A NCBI36
NG_016621.2:g.10481T>A

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-354T>A
NR_033319.2:n.174-354T>A
NR_033320.2:n.174-354T>A
NR_033321.2:n.174-354T>A
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