Canonical Allele Identifier: CA2378754353
Gene: MIR99AHG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.16295399T= , CM000683.2:g.16295399T= GRCh38
NC_000021.8:g.17667720T= , CM000683.1:g.17667720T= GRCh37
NC_000021.7:g.16589591T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027790.2:n.469+64284T=
NR_027790.3:n.469+64284T=
NR_027791.2:n.315+64284T=
NR_027791.3:n.315+64284T=
NR_111004.1:n.442+64284T=
NR_111004.2:n.442+64284T=
NR_111005.1:n.442+64284T=
NR_111005.2:n.442+64284T=
NR_136541.1:n.522+64284T=
NR_136542.1:n.522+64284T=
NR_136543.1:n.315+64284T=
NR_136551.1:n.350+64284T=
NR_136552.1:n.350+64284T=