Canonical Allele Identifier: CA752042710
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1355760913

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662975T>C , CM000684.2:g.26662975T>C GRCh38
NC_000022.10:g.27058939T>C , CM000684.1:g.27058939T>C GRCh37
NC_000022.9:g.25388939T>C NCBI36
NG_016621.2:g.10494T>C

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-341T>C
NR_033319.2:n.174-341T>C
NR_033320.2:n.174-341T>C
NR_033321.2:n.174-341T>C