Canonical Allele Identifier: CA753659581

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs1376453259
• gnomAD v3: 22-46108497-G-A
• gnomAD v4: 22-46108497-G-A
• MyVariant Identifiers: chr22:g.46504377G>A (hg19) ; chr22:g.46108497G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108497G>A , CM000684.2:g.46108497G>A	GRCh38
NC_000022.10:g.46504377G>A , CM000684.1:g.46504377G>A	GRCh37
NC_000022.9:g.44883041G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-770G>A
NR_110479.1:n.315-770G>A