Canonical Allele Identifier: CA5011535
Gene: IFNE HGNC NCBI
MIR31HG HGNC NCBI
COSMIC:
COSM4416494 (not active)
MyVariant.info:
GRCh38 chr9:g.21481484G>A
GRCh37 chr9:g.21481483G>A
gnomAD v2:
9:21481483 G / A
gnomAD v3:
9:21481484 G / A
gnomAD v4:
chr9-21481484-G-A
Joint Max Group AF 0.17860403 (EAS)
Genomes Max Group AF 0.17252746 (EAS)
Exomes Max Group AF 0.17836159 (EAS)
dbSNP:
2039381
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21481484G>A , CM000671.2:g.21481484G>A GRCh38
NC_000009.11:g.21481483G>A , CM000671.1:g.21481483G>A GRCh37
NC_000009.10:g.21471483G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000448696.4:c.211C>T (IFNE) MANE Select ENSP00000418018.2:p.Gln71Ter
NM_176891.4:c.211C>T (IFNE) NP_795372.1:p.Gln71Ter
NR_027054.1:n.211-4192C>T (MIR31HG)
NR_027054.2:n.311-4192C>T (MIR31HG)
NR_152877.1:n.52-4192C>T (MIR31HG)
NR_152878.1:n.52-4192C>T (MIR31HG)
NR_152879.1:n.311-4192C>T (MIR31HG)
NM_176891.5:c.211C>T (IFNE) MANE Select NP_795372.1:p.Gln71Ter
Search 100 bp 5'
Search 100 bp 3'