Canonical Allele Identifier: CA505675883
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

dbSNP Id: rs1599627623
MyVariant Identifiers: chr19:g.13947308A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.24T>C (MIR27A)
NR_036515.2:n.6425T>C (MIR23AHG)