Canonical Allele Identifier: CA16003564
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs2301523

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26666705G>A , CM000684.2:g.26666705G>A GRCh38
NC_000022.10:g.27062669G>A , CM000684.1:g.27062669G>A GRCh37
NC_000022.9:g.25392669G>A NCBI36
NG_016621.2:g.14224G>A

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.1505G>A
NR_033319.2:n.1505G>A
NR_033320.2:n.1431G>A
NR_033321.2:n.1431G>A