Canonical Allele Identifier: CA589477110
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1363260082

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167211_94167213del , CM000671.2:g.94167211_94167213del GRCh38
NC_000009.11:g.96929493_96929495del , CM000671.1:g.96929493_96929495del GRCh37
NC_000009.10:g.95969314_95969316del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+830_124+832del
NR_170275.1:n.124+830_124+832del
NR_170276.1:n.124+830_124+832del
NR_170277.1:n.124+830_124+832del
NR_170278.1:n.124+830_124+832del