Canonical Allele Identifier: CA2378831733
Gene: MIR99AHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.16455971A= , CM000683.2:g.16455971A= GRCh38
NC_000021.8:g.17828291A= , CM000683.1:g.17828291A= GRCh37
NC_000021.7:g.16750162A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027790.2:n.470-31519A=
NR_027790.3:n.470-31519A=
NR_027791.2:n.388-31519A=
NR_027791.3:n.388-31519A=
NR_111004.1:n.515-31519A=
NR_111004.2:n.515-31519A=
NR_111005.1:n.515-31519A=
NR_111005.2:n.515-31519A=
NR_136541.1:n.595-31519A=
NR_136542.1:n.595-31519A=
NR_136543.1:n.388-31519A=
NR_136544.1:n.540-31519A=
NR_136545.1:n.540-31519A=
NR_136546.1:n.540-31519A=
NR_136550.1:n.279-31519A=
NR_136551.1:n.423-31519A=
NR_136552.1:n.423-31519A=