Canonical Allele Identifier: CA9243209
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

dbSNP Id: rs11671784
ExAC: 19:13947296 G / A
gnomAD v2: 19-13947296-G-A
gnomAD v3: 19-13836482-G-A
gnomAD v4: 19-13836482-G-A
MyVariant Identifiers: chr19:g.13947296G>A (hg19) chr19:g.13836482G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.36C>T (MIR27A)
NR_036515.2:n.6437C>T (MIR23AHG)
Search 100 bp 5'
Search 100 bp 3'