Canonical Allele Identifier: CA2720226020
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs2118235937

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166948_94166950del , CM000671.2:g.94166948_94166950del GRCh38
NC_000009.11:g.96929230_96929232del , CM000671.1:g.96929230_96929232del GRCh37
NC_000009.10:g.95969051_95969053del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+567_124+569del
NR_170275.1:n.124+567_124+569del
NR_170276.1:n.124+567_124+569del
NR_170277.1:n.124+567_124+569del
NR_170278.1:n.124+567_124+569del