Canonical Allele Identifier: CA980689293

Gene: MIR22HG

Linked Data

• dbSNP Id: rs1914426769
• gnomAD v3: 17-1714969-A-T
• gnomAD v4: 17-1714969-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1714969A>T , CM000679.2:g.1714969A>T	GRCh38
NC_000017.10:g.1618263A>T , CM000679.1:g.1618263A>T	GRCh37
NC_000017.9:g.1565013A>T	NCBI36
NG_032811.1:g.3447A>T

Transcript Alleles

HGVS	Amino-acid Change
NR_028502.1:n.144-955T>A
NR_028503.1:n.144-955T>A
NR_028504.1:n.144-516T>A
NR_028505.1:n.144-955T>A