Canonical Allele Identifier: CA639631550
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1259706310

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46111693C>T , CM000684.2:g.46111693C>T GRCh38
NC_000022.10:g.46507573C>T , CM000684.1:g.46507573C>T GRCh37
NC_000022.9:g.44886237C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.2482C>T
NR_110479.1:n.2331C>T