Canonical Allele Identifier: CA505675861
Gene: MIR27A HGNC NCBI
MIR23AHG HGNC NCBI

Linked Data

gnomAD v4: 19-13836487-T-C
MyVariant Identifiers: chr19:g.13947301T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.13836487T>C , CM000681.2:g.13836487T>C GRCh38
NC_000019.9:g.13947301T>C , CM000681.1:g.13947301T>C GRCh37
NC_000019.8:g.13808301T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_029501.1:n.31A>G (MIR27A)
NR_036515.2:n.6432A>G (MIR23AHG)
Search 100 bp 5'
Search 100 bp 3'