Canonical Allele Identifier: CA2838488450
Gene: MIR3171HG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.27293254C>A , CM000676.2:g.27293254C>A GRCh38
NC_000014.8:g.27762460C>A , CM000676.1:g.27762460C>A GRCh37
NC_000014.7:g.26832300C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000553392.5:n.528+17769G>T
Search 100 bp 5'
Search 100 bp 3'