Canonical Allele Identifier: CA325105822

Gene: MIRLET7BHG

Linked Data

• dbSNP Id: rs906005918
• MyVariant Identifiers: chr22:g.46504322C>G (hg19) ; chr22:g.46108442C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46108442C>G , CM000684.2:g.46108442C>G	GRCh38
NC_000022.10:g.46504322C>G , CM000684.1:g.46504322C>G	GRCh37
NC_000022.9:g.44882986C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027033.2:n.373-825C>G
NR_110479.1:n.315-825C>G