Canonical Allele Identifier: CA512491034
Gene: AIRE HGNC NCBI

Linked Data

ClinVar Variation Id: 2029834
ClinVar RCV Id: RCV002894254
MyVariant Identifiers: chr21:g.45709676C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44289793C>G , CM000683.2:g.44289793C>G GRCh38
NC_000021.8:g.45709676C>G , CM000683.1:g.45709676C>G GRCh37
NC_000021.7:g.44534104C>G NCBI36
NG_009556.1:g.8914C>G , LRG_18:g.8914C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.789C>G MANE Select ENSP00000291582.5:p.Gly263=
ENST00000291582.5:c.789C>G ENSP00000291582.5:p.Gly263=
ENST00000527919.5:n.1522C>G
ENST00000530812.5:n.2539C>G
NM_000383.3:c.789C>G NP_000374.1:p.Gly263=
XM_011529551.1:c.789C>G XP_011527853.1:p.Gly263=
NM_000383.4:c.789C>G MANE Select NP_000374.1:p.Gly263=
Search 100 bp 5'
Search 100 bp 3'