Canonical Allele Identifier: CA10051736
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs764002506
ExAC: 21:45709873 T / C
gnomAD v2: 21-45709873-T-C
gnomAD v4: 21-44289990-T-C
MyVariant Identifiers: chr21:g.45709873T>C (hg19) chr21:g.44289990T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44289990T>C , CM000683.2:g.44289990T>C GRCh38
NC_000021.8:g.45709873T>C , CM000683.1:g.45709873T>C GRCh37
NC_000021.7:g.44534301T>C NCBI36
NG_009556.1:g.9111T>C , LRG_18:g.9111T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.801T>C MANE Select ENSP00000291582.5:p.Gly267=
ENST00000291582.5:c.801T>C ENSP00000291582.5:p.Gly267=
ENST00000527919.5:n.1534T>C
ENST00000530812.5:n.2551T>C
NM_000383.3:c.801T>C NP_000374.1:p.Gly267=
XM_011529551.1:c.801T>C XP_011527853.1:p.Gly267=
NM_000383.4:c.801T>C MANE Select NP_000374.1:p.Gly267=
Search 100 bp 5'
Search 100 bp 3'