Canonical Allele Identifier: CA868687628
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1353654399
MyVariant Identifiers: chr9:g.96929316_96929332del (hg19) chr9:g.94167034_94167050del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167042_94167058del , CM000671.2:g.94167042_94167058del GRCh38
NC_000009.11:g.96929324_96929340del , CM000671.1:g.96929324_96929340del GRCh37
NC_000009.10:g.95969145_95969161del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+661_124+677del
NR_170275.1:n.124+661_124+677del
NR_170276.1:n.124+661_124+677del
NR_170277.1:n.124+661_124+677del
NR_170278.1:n.124+661_124+677del
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