Canonical Allele Identifier: CA512491017
Gene: AIRE HGNC NCBI

Linked Data

ClinVar Variation Id: 1161537
ClinVar RCV Id: RCV001506090
dbSNP Id: rs2040517869
MyVariant Identifiers: chr21:g.45709661C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44289778C>T , CM000683.2:g.44289778C>T GRCh38
NC_000021.8:g.45709661C>T , CM000683.1:g.45709661C>T GRCh37
NC_000021.7:g.44534089C>T NCBI36
NG_009556.1:g.8899C>T , LRG_18:g.8899C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.774C>T MANE Select ENSP00000291582.5:p.Ala258=
ENST00000291582.5:c.774C>T ENSP00000291582.5:p.Ala258=
ENST00000527919.5:n.1507C>T
ENST00000530812.5:n.2524C>T
NM_000383.3:c.774C>T NP_000374.1:p.Ala258=
XM_011529551.1:c.774C>T XP_011527853.1:p.Ala258=
NM_000383.4:c.774C>T MANE Select NP_000374.1:p.Ala258=
Search 100 bp 5'
Search 100 bp 3'