Canonical Allele Identifier: CA752042691
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1253048995

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662916_26662921del , CM000684.2:g.26662916_26662921del GRCh38
NC_000022.10:g.27058880_27058885del , CM000684.1:g.27058880_27058885del GRCh37
NC_000022.9:g.25388880_25388885del NCBI36
NG_016621.2:g.10435_10440del

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-400_174-395del
NR_033319.2:n.174-400_174-395del
NR_033320.2:n.174-400_174-395del
NR_033321.2:n.174-400_174-395del