Canonical Allele Identifier: CA325105827

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs34212001
• gnomAD v2: 22-46504336-CT-C
• gnomAD v3: 22-46108456-CT-C
• gnomAD v4: 22-46108456-CT-C
• MyVariant Identifiers: chr22:g.46504337del (hg19) ; chr22:g.46108457del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108457del , CM000684.2:g.46108457del	GRCh38
NC_000022.10:g.46504337del , CM000684.1:g.46504337del	GRCh37
NC_000022.9:g.44883001del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-810del
NR_110479.1:n.315-810del