Canonical Allele Identifier: CA638869679
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1180053992

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662775C>T , CM000684.2:g.26662775C>T GRCh38
NC_000022.10:g.27058739C>T , CM000684.1:g.27058739C>T GRCh37
NC_000022.9:g.25388739C>T NCBI36
NG_016621.2:g.10294C>T

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-541C>T
NR_033319.2:n.174-541C>T
NR_033320.2:n.174-541C>T
NR_033321.2:n.174-541C>T