Canonical Allele Identifier: CA2552288355
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662833C>T , CM000684.2:g.26662833C>T GRCh38
NC_000022.10:g.27058797C>T , CM000684.1:g.27058797C>T GRCh37
NC_000022.9:g.25388797C>T NCBI36
NG_016621.2:g.10352C>T

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-483C>T
NR_033319.2:n.174-483C>T
NR_033320.2:n.174-483C>T
NR_033321.2:n.174-483C>T