Canonical Allele Identifier: CA753662088
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1193904668

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46111603C>T , CM000684.2:g.46111603C>T GRCh38
NC_000022.10:g.46507483C>T , CM000684.1:g.46507483C>T GRCh37
NC_000022.9:g.44886147C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.2392C>T
NR_110479.1:n.2241C>T