Canonical Allele Identifier: CA2818611688
Gene: MIAT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662948C>A , CM000684.2:g.26662948C>A GRCh38
NC_000022.10:g.27058912C>A , CM000684.1:g.27058912C>A GRCh37
NC_000022.9:g.25388912C>A NCBI36
NG_016621.2:g.10467C>A

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-368C>A
NR_033319.2:n.174-368C>A
NR_033320.2:n.174-368C>A
NR_033321.2:n.174-368C>A
Search 100 bp 5'
Search 100 bp 3'