Canonical Allele Identifier: CA2399297379
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1930719894

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662779A>C , CM000684.2:g.26662779A>C GRCh38
NC_000022.10:g.27058743A>C , CM000684.1:g.27058743A>C GRCh37
NC_000022.9:g.25388743A>C NCBI36
NG_016621.2:g.10298A>C

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-537A>C
NR_033319.2:n.174-537A>C
NR_033320.2:n.174-537A>C
NR_033321.2:n.174-537A>C