Canonical Allele Identifier: CA868687598
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs62578777
gnomAD v3: 9-94167001-C-A
gnomAD v4: 9-94167001-C-A
MyVariant Identifiers: chr9:g.96929283C>A (hg19) chr9:g.94167001C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167001C>A , CM000671.2:g.94167001C>A GRCh38
NC_000009.11:g.96929283C>A , CM000671.1:g.96929283C>A GRCh37
NC_000009.10:g.95969104C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+620C>A
NR_170275.1:n.124+620C>A
NR_170276.1:n.124+620C>A
NR_170277.1:n.124+620C>A
NR_170278.1:n.124+620C>A
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