Canonical Allele Identifier: CA2408583969
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1922852529

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108565C>T , CM000684.2:g.46108565C>T GRCh38
NC_000022.10:g.46504445C>T , CM000684.1:g.46504445C>T GRCh37
NC_000022.9:g.44883109C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-702C>T
NR_110479.1:n.315-702C>T