Canonical Allele Identifier: CA1026264660
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1922845879

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46108444T>C , CM000684.2:g.46108444T>C GRCh38
NC_000022.10:g.46504324T>C , CM000684.1:g.46504324T>C GRCh37
NC_000022.9:g.44882988T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027033.2:n.373-823T>C
NR_110479.1:n.315-823T>C