Canonical Allele Identifier: CA639631529
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1397689505

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46111615G>C , CM000684.2:g.46111615G>C GRCh38
NC_000022.10:g.46507495G>C , CM000684.1:g.46507495G>C GRCh37
NC_000022.9:g.44886159G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.2404G>C
NR_110479.1:n.2253G>C