Canonical Allele Identifier: CA505675880
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

gnomAD v4: 19-13836493-C-A
MyVariant Identifiers: chr19:g.13947307C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13836493C>A , CM000681.2:g.13836493C>A GRCh38
NC_000019.9:g.13947307C>A , CM000681.1:g.13947307C>A GRCh37
NC_000019.8:g.13808307C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.25G>T (MIR27A)
NR_036515.2:n.6426G>T (MIR23AHG)
Search 100 bp 5'
Search 100 bp 3'