Canonical Allele Identifier: CA2399299192
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26666705G= , CM000684.2:g.26666705G= GRCh38
NC_000022.10:g.27062669G= , CM000684.1:g.27062669G= GRCh37
NC_000022.9:g.25392669G= NCBI36
NG_016621.2:g.14224G=

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.1505G=
NR_033319.2:n.1505G=
NR_033320.2:n.1431G=
NR_033321.2:n.1431G=