Canonical Allele Identifier: CA505675846
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.13947296G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13836482G>T , CM000681.2:g.13836482G>T GRCh38
NC_000019.9:g.13947296G>T , CM000681.1:g.13947296G>T GRCh37
NC_000019.8:g.13808296G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.36C>A (MIR27A)
NR_036515.2:n.6437C>A (MIR23AHG)