Canonical Allele Identifier: CA325105846

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs34829149
• gnomAD v2: 22-46504359-T-C
• gnomAD v3: 22-46108479-T-C
• gnomAD v4: 22-46108479-T-C
• MyVariant Identifiers: chr22:g.46504359T>C (hg19) ; chr22:g.46108479T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108479T>C , CM000684.2:g.46108479T>C	GRCh38
NC_000022.10:g.46504359T>C , CM000684.1:g.46504359T>C	GRCh37
NC_000022.9:g.44883023T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-788T>C
NR_110479.1:n.315-788T>C