Canonical Allele Identifier: CA286856124
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs764460581
gnomAD v3: 17-1715060-G-C
gnomAD v4: 17-1715060-G-C
MyVariant Identifiers: chr17:g.1618354G>C (hg19) chr17:g.1715060G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715060G>C , CM000679.2:g.1715060G>C GRCh38
NC_000017.10:g.1618354G>C , CM000679.1:g.1618354G>C GRCh37
NC_000017.9:g.1565104G>C NCBI36
NG_032811.1:g.3538G>C

Transcript Alleles

HGVS Amino-acid Change
NR_028502.1:n.144-1046C>G
NR_028503.1:n.144-1046C>G
NR_028504.1:n.144-607C>G
NR_028505.1:n.144-1046C>G
Search 100 bp 5'
Search 100 bp 3'