Canonical Allele Identifier: CA2544476748
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662976C>G , CM000684.2:g.26662976C>G GRCh38
NC_000022.10:g.27058940C>G , CM000684.1:g.27058940C>G GRCh37
NC_000022.9:g.25388940C>G NCBI36
NG_016621.2:g.10495C>G

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-340C>G
NR_033319.2:n.174-340C>G
NR_033320.2:n.174-340C>G
NR_033321.2:n.174-340C>G