Canonical Allele Identifier: CA373082609
Gene: IFNE HGNC NCBI
MIR31HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21481557T>A , CM000671.2:g.21481557T>A GRCh38
NC_000009.11:g.21481556T>A , CM000671.1:g.21481556T>A GRCh37
NC_000009.10:g.21471556T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000448696.4:c.138A>T (IFNE) MANE Select ENSP00000418018.2:p.Gln46His
NM_176891.4:c.138A>T (IFNE) NP_795372.1:p.Gln46His
NR_027054.1:n.211-4265A>T (MIR31HG)
NR_027054.2:n.311-4265A>T (MIR31HG)
NR_152877.1:n.52-4265A>T (MIR31HG)
NR_152878.1:n.52-4265A>T (MIR31HG)
NR_152879.1:n.311-4265A>T (MIR31HG)
NM_176891.5:c.138A>T (IFNE) MANE Select NP_795372.1:p.Gln46His