Canonical Allele Identifier: CA2242998162
Gene: MIR22HG HGNC NCBI

Linked Data

dbSNP Id: rs1914435848

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1715072A>C , CM000679.2:g.1715072A>C GRCh38
NC_000017.10:g.1618366A>C , CM000679.1:g.1618366A>C GRCh37
NC_000017.9:g.1565116A>C NCBI36
NG_032811.1:g.3550A>C

Transcript Alleles

HGVS Amino-acid change
NR_028502.1:n.144-1058T>G
NR_028503.1:n.144-1058T>G
NR_028504.1:n.144-619T>G
NR_028505.1:n.144-1058T>G