Canonical Allele Identifier: CA752042671
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1332134795

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662804A>T , CM000684.2:g.26662804A>T GRCh38
NC_000022.10:g.27058768A>T , CM000684.1:g.27058768A>T GRCh37
NC_000022.9:g.25388768A>T NCBI36
NG_016621.2:g.10323A>T

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-512A>T
NR_033319.2:n.174-512A>T
NR_033320.2:n.174-512A>T
NR_033321.2:n.174-512A>T