Canonical Allele Identifier: CA1026266570
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1923002557

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46111697A>C , CM000684.2:g.46111697A>C GRCh38
NC_000022.10:g.46507577A>C , CM000684.1:g.46507577A>C GRCh37
NC_000022.9:g.44886241A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.2486A>C
NR_110479.1:n.2335A>C