Canonical Allele Identifier: CA1026266199
Gene: MIRLET7BHG HGNC NCBI

Linked Data

dbSNP Id: rs1922995859

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.46111607C>T , CM000684.2:g.46111607C>T GRCh38
NC_000022.10:g.46507487C>T , CM000684.1:g.46507487C>T GRCh37
NC_000022.9:g.44886151C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_027033.2:n.2396C>T
NR_110479.1:n.2245C>T