Canonical Allele Identifier: CA1024749533
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1930719545

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662774C>T , CM000684.2:g.26662774C>T GRCh38
NC_000022.10:g.27058738C>T , CM000684.1:g.27058738C>T GRCh37
NC_000022.9:g.25388738C>T NCBI36
NG_016621.2:g.10293C>T

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-542C>T
NR_033319.2:n.174-542C>T
NR_033320.2:n.174-542C>T
NR_033321.2:n.174-542C>T