Canonical Allele Identifier: CA639630716

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs1456442389
• gnomAD v2: 22-46504432-C-T
• gnomAD v3: 22-46108552-C-T
• gnomAD v4: 22-46108552-C-T
• MyVariant Identifiers: chr22:g.46504432C>T (hg19) ; chr22:g.46108552C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108552C>T , CM000684.2:g.46108552C>T	GRCh38
NC_000022.10:g.46504432C>T , CM000684.1:g.46504432C>T	GRCh37
NC_000022.9:g.44883096C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-715C>T
NR_110479.1:n.315-715C>T