Canonical Allele Identifier: CA2399297404
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662849C= , CM000684.2:g.26662849C= GRCh38
NC_000022.10:g.27058813C= , CM000684.1:g.27058813C= GRCh37
NC_000022.9:g.25388813C= NCBI36
NG_016621.2:g.10368C=

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-467C=
NR_033319.2:n.174-467C=
NR_033320.2:n.174-467C=
NR_033321.2:n.174-467C=