Canonical Allele Identifier: CA747303387

Gene: MIR99AHG

Linked Data

• dbSNP Id: rs2823743
• MyVariant Identifiers: chr21:g.17667720T>A (hg19) ; chr21:g.16295399T>A (hg38)

Genomic Alleles

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

Transcript Alleles

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