Canonical Allele Identifier: CA10051634
Gene: AIRE HGNC NCBI

Linked Data

ClinVar Variation Id: 495854
ClinVar RCV Id: RCV000586806 RCV001834836
dbSNP Id: rs148012328
ExAC: 21:45708278 G / A
gnomAD v2: 21-45708278-G-A
gnomAD v3: 21-44288395-G-A
gnomAD v4: 21-44288395-G-A
MyVariant Identifiers: chr21:g.45708278G>A (hg19) chr21:g.44288395G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44288395G>A , CM000683.2:g.44288395G>A GRCh38
NC_000021.8:g.45708278G>A , CM000683.1:g.45708278G>A GRCh37
NC_000021.7:g.44532706G>A NCBI36
NG_009556.1:g.7516G>A , LRG_18:g.7516G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.589G>A MANE Select ENSP00000291582.5:p.Gly197Arg
ENST00000291582.5:c.589G>A ENSP00000291582.5:p.Gly197Arg
ENST00000527919.5:n.1133G>A
ENST00000530812.5:n.1141G>A
NM_000383.3:c.589G>A NP_000374.1:p.Gly197Arg
XM_011529551.1:c.589G>A XP_011527853.1:p.Gly197Arg
NM_000383.4:c.589G>A MANE Select NP_000374.1:p.Gly197Arg
Search 100 bp 5'
Search 100 bp 3'