Canonical Allele Identifier: CA196508843
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1009264487
MyVariant Identifiers: chr9:g.96929208_96929230del (hg19) chr9:g.94166926_94166948del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166931_94166953del , CM000671.2:g.94166931_94166953del GRCh38
NC_000009.11:g.96929213_96929235del , CM000671.1:g.96929213_96929235del GRCh37
NC_000009.10:g.95969034_95969056del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+550_124+572del
NR_170275.1:n.124+550_124+572del
NR_170276.1:n.124+550_124+572del
NR_170277.1:n.124+550_124+572del
NR_170278.1:n.124+550_124+572del
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