Canonical Allele Identifier: CA505675886

Gene: MIR27A MIR23AHG

Linked Data

• dbSNP Id: rs1599627626
• MyVariant Identifiers: chr19:g.13947309A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.13836495A>G , CM000681.2:g.13836495A>G	GRCh38
NC_000019.9:g.13947309A>G , CM000681.1:g.13947309A>G	GRCh37
NC_000019.8:g.13808309A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_029501.1:n.23T>C (MIR27A)
NR_036515.2:n.6424T>C (MIR23AHG)