Canonical Allele Identifier: CA980689326

Gene: MIR22HG

Linked Data

• dbSNP Id: rs1914436005
• gnomAD v3: 17-1715074-C-T
• gnomAD v4: 17-1715074-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1715074C>T , CM000679.2:g.1715074C>T	GRCh38
NC_000017.10:g.1618368C>T , CM000679.1:g.1618368C>T	GRCh37
NC_000017.9:g.1565118C>T	NCBI36
NG_032811.1:g.3552C>T

Transcript Alleles

HGVS	Amino-acid change
NR_028502.1:n.143+1056G>A
NR_028503.1:n.143+1056G>A
NR_028504.1:n.144-621G>A
NR_028505.1:n.143+1056G>A