Canonical Allele Identifier: CA2563581358
Gene: MIAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662979C>A , CM000684.2:g.26662979C>A GRCh38
NC_000022.10:g.27058943C>A , CM000684.1:g.27058943C>A GRCh37
NC_000022.9:g.25388943C>A NCBI36
NG_016621.2:g.10498C>A

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-337C>A
NR_033319.2:n.174-337C>A
NR_033320.2:n.174-337C>A
NR_033321.2:n.174-337C>A
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