Canonical Allele Identifier: CA196508863
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs747991999
MyVariant Identifiers: chr9:g.96929243_96929264del (hg19) chr9:g.94166961_94166982del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94166962_94166983del , CM000671.2:g.94166962_94166983del GRCh38
NC_000009.11:g.96929244_96929265del , CM000671.1:g.96929244_96929265del GRCh37
NC_000009.10:g.95969065_95969086del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+581_124+602del
NR_170275.1:n.124+581_124+602del
NR_170276.1:n.124+581_124+602del
NR_170277.1:n.124+581_124+602del
NR_170278.1:n.124+581_124+602del
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