Canonical Allele Identifier: CA196509113
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs867176325
gnomAD v3: 9-94167465-T-G
gnomAD v4: 9-94167465-T-G
MyVariant Identifiers: chr9:g.96929747T>G (hg19) chr9:g.94167465T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167465T>G , CM000671.2:g.94167465T>G GRCh38
NC_000009.11:g.96929747T>G , CM000671.1:g.96929747T>G GRCh37
NC_000009.10:g.95969568T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1084T>G
NR_170275.1:n.124+1084T>G
NR_170276.1:n.124+1084T>G
NR_170277.1:n.124+1084T>G
NR_170278.1:n.124+1084T>G
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