Canonical Allele Identifier: CA752042674
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1393017851

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662812C>A , CM000684.2:g.26662812C>A GRCh38
NC_000022.10:g.27058776C>A , CM000684.1:g.27058776C>A GRCh37
NC_000022.9:g.25388776C>A NCBI36
NG_016621.2:g.10331C>A

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-504C>A
NR_033319.2:n.174-504C>A
NR_033320.2:n.174-504C>A
NR_033321.2:n.174-504C>A