Canonical Allele Identifier: CA505675884
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.13947308A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13836494A>T , CM000681.2:g.13836494A>T GRCh38
NC_000019.9:g.13947308A>T , CM000681.1:g.13947308A>T GRCh37
NC_000019.8:g.13808308A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.24T>A (MIR27A)
NR_036515.2:n.6425T>A (MIR23AHG)
Search 100 bp 5'
Search 100 bp 3'