Canonical Allele Identifier: CA1126885714
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs2118235893

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166944_94166950del , CM000671.2:g.94166944_94166950del GRCh38
NC_000009.11:g.96929226_96929232del , CM000671.1:g.96929226_96929232del GRCh37
NC_000009.10:g.95969047_95969053del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+563_124+569del
NR_170275.1:n.124+563_124+569del
NR_170276.1:n.124+563_124+569del
NR_170277.1:n.124+563_124+569del
NR_170278.1:n.124+563_124+569del