Canonical Allele Identifier: CA2399297447
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662968C= , CM000684.2:g.26662968C= GRCh38
NC_000022.10:g.27058932C= , CM000684.1:g.27058932C= GRCh37
NC_000022.9:g.25388932C= NCBI36
NG_016621.2:g.10487C=

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-348C=
NR_033319.2:n.174-348C=
NR_033320.2:n.174-348C=
NR_033321.2:n.174-348C=