Canonical Allele Identifier: CA2399297436
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1930724697

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662939G>A , CM000684.2:g.26662939G>A GRCh38
NC_000022.10:g.27058903G>A , CM000684.1:g.27058903G>A GRCh37
NC_000022.9:g.25388903G>A NCBI36
NG_016621.2:g.10458G>A

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-377G>A
NR_033319.2:n.174-377G>A
NR_033320.2:n.174-377G>A
NR_033321.2:n.174-377G>A