Canonical Allele Identifier: CA505675870
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.13947304T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13836490T>A , CM000681.2:g.13836490T>A GRCh38
NC_000019.9:g.13947304T>A , CM000681.1:g.13947304T>A GRCh37
NC_000019.8:g.13808304T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.28A>T (MIR27A)
NR_036515.2:n.6429A>T (MIR23AHG)