Canonical Allele Identifier: CA752042658
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662764del , CM000684.2:g.26662764del GRCh38
NC_000022.10:g.27058728del , CM000684.1:g.27058728del GRCh37
NC_000022.9:g.25388728del NCBI36
NG_016621.2:g.10283del

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-552del
NR_033319.2:n.174-552del
NR_033320.2:n.174-552del
NR_033321.2:n.174-552del