Canonical Allele Identifier: CA2818611685
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662814G>T , CM000684.2:g.26662814G>T GRCh38
NC_000022.10:g.27058778G>T , CM000684.1:g.27058778G>T GRCh37
NC_000022.9:g.25388778G>T NCBI36
NG_016621.2:g.10333G>T

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-502G>T
NR_033319.2:n.174-502G>T
NR_033320.2:n.174-502G>T
NR_033321.2:n.174-502G>T