Canonical Allele Identifier: CA196509122
Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs1013489803
MyVariant Identifiers: chr9:g.96929820G>T (hg19) chr9:g.94167538G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.94167538G>T , CM000671.2:g.94167538G>T GRCh38
NC_000009.11:g.96929820G>T , CM000671.1:g.96929820G>T GRCh37
NC_000009.10:g.95969641G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_170274.1:n.124+1157G>T
NR_170275.1:n.124+1157G>T
NR_170276.1:n.124+1157G>T
NR_170277.1:n.124+1157G>T
NR_170278.1:n.124+1157G>T
Search 100 bp 5'
Search 100 bp 3'