Canonical Allele Identifier: CA2739302886
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662857C>G , CM000684.2:g.26662857C>G GRCh38
NC_000022.10:g.27058821C>G , CM000684.1:g.27058821C>G GRCh37
NC_000022.9:g.25388821C>G NCBI36
NG_016621.2:g.10376C>G

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-459C>G
NR_033319.2:n.174-459C>G
NR_033320.2:n.174-459C>G
NR_033321.2:n.174-459C>G