Canonical Allele Identifier: CA980689337

Gene: MIR22HG

Linked Data

• dbSNP Id: rs975986521
• gnomAD v3: 17-1715097-G-C
• gnomAD v4: 17-1715097-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1715097G>C , CM000679.2:g.1715097G>C	GRCh38
NC_000017.10:g.1618391G>C , CM000679.1:g.1618391G>C	GRCh37
NC_000017.9:g.1565141G>C	NCBI36
NG_032811.1:g.3575G>C

Transcript Alleles

HGVS	Amino-acid change
NR_028502.1:n.143+1033C>G
NR_028503.1:n.143+1033C>G
NR_028504.1:n.144-644C>G
NR_028505.1:n.143+1033C>G