Canonical Allele Identifier: CA639630731

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs1385385695
• gnomAD v2: 22-46504448-C-T
• gnomAD v3: 22-46108568-C-T
• gnomAD v4: 22-46108568-C-T
• MyVariant Identifiers: chr22:g.46504448C>T (hg19) ; chr22:g.46108568C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108568C>T , CM000684.2:g.46108568C>T	GRCh38
NC_000022.10:g.46504448C>T , CM000684.1:g.46504448C>T	GRCh37
NC_000022.9:g.44883112C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-699C>T
NR_110479.1:n.315-699C>T