Canonical Allele Identifier: CA512490188
Gene: AIRE HGNC NCBI

Linked Data

ClinVar Variation Id: 2154425
ClinVar RCV Id: RCV003081778
gnomAD v4: 21-44286661-G-A
MyVariant Identifiers: chr21:g.45706544G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44286661G>A , CM000683.2:g.44286661G>A GRCh38
NC_000021.8:g.45706544G>A , CM000683.1:g.45706544G>A GRCh37
NC_000021.7:g.44530972G>A NCBI36
NG_009556.1:g.5782G>A , LRG_18:g.5782G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000291582.6:c.237G>A MANE Select ENSP00000291582.5:p.Arg79=
ENST00000291582.5:c.237G>A ENSP00000291582.5:p.Arg79=
ENST00000527919.5:n.398G>A
ENST00000530812.5:n.406G>A
NM_000383.3:c.237G>A NP_000374.1:p.Arg79=
XM_011529551.1:c.237G>A XP_011527853.1:p.Arg79=
NM_000383.4:c.237G>A MANE Select NP_000374.1:p.Arg79=
Search 100 bp 5'
Search 100 bp 3'