Canonical Allele Identifier: CA752042661
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1317321702

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662777A>G , CM000684.2:g.26662777A>G GRCh38
NC_000022.10:g.27058741A>G , CM000684.1:g.27058741A>G GRCh37
NC_000022.9:g.25388741A>G NCBI36
NG_016621.2:g.10296A>G

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-539A>G
NR_033319.2:n.174-539A>G
NR_033320.2:n.174-539A>G
NR_033321.2:n.174-539A>G