Canonical Allele Identifier: CA286856206

Gene: MIR22HG

Linked Data

• dbSNP Id: rs775049141
• gnomAD v3: 17-1715104-C-G
• gnomAD v4: 17-1715104-C-G
• MyVariant Identifiers: chr17:g.1618398C>G (hg19) ; chr17:g.1715104C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1715104C>G , CM000679.2:g.1715104C>G	GRCh38
NC_000017.10:g.1618398C>G , CM000679.1:g.1618398C>G	GRCh37
NC_000017.9:g.1565148C>G	NCBI36
NG_032811.1:g.3582C>G

Transcript Alleles

HGVS	Amino-acid change
NR_028502.1:n.143+1026G>C
NR_028503.1:n.143+1026G>C
NR_028504.1:n.144-651G>C
NR_028505.1:n.143+1026G>C