Canonical Allele Identifier: CA321793341
Gene: AIRE HGNC NCBI

Linked Data

ClinVar Variation Id: 2886891
ClinVar RCV Id: RCV003635882
dbSNP Id: rs765356727
gnomAD v2: 21-45709971-G-A
gnomAD v3: 21-44290088-G-A
gnomAD v4: 21-44290088-G-A
MyVariant Identifiers: chr21:g.45709971G>A (hg19) chr21:g.44290088G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44290088G>A , CM000683.2:g.44290088G>A GRCh38
NC_000021.8:g.45709971G>A , CM000683.1:g.45709971G>A GRCh37
NC_000021.7:g.44534399G>A NCBI36
NG_009556.1:g.9209G>A , LRG_18:g.9209G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.879+20G>A MANE Select ENSP00000291582.5:n.879+20G>A
ENST00000291582.5:c.879+20G>A ENSP00000291582.5:n.879+20G>A
ENST00000527919.5:n.1612+20G>A
ENST00000530812.5:n.2629+20G>A
NM_000383.3:c.879+20G>A NP_000374.1:n.879+20G>A
XM_011529551.1:c.879+20G>A XP_011527853.1:n.879+20G>A
NM_000383.4:c.879+20G>A MANE Select NP_000374.1:n.879+20G>A
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