Canonical Allele Identifier: CA752042679
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1427482809

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662840C>T , CM000684.2:g.26662840C>T GRCh38
NC_000022.10:g.27058804C>T , CM000684.1:g.27058804C>T GRCh37
NC_000022.9:g.25388804C>T NCBI36
NG_016621.2:g.10359C>T

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-476C>T
NR_033319.2:n.174-476C>T
NR_033320.2:n.174-476C>T
NR_033321.2:n.174-476C>T