Canonical Allele Identifier: CA749676953
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs1448069210
gnomAD v3: 21-44287356-C-T
gnomAD v4: 21-44287356-C-T
MyVariant Identifiers: chr21:g.45707239C>T (hg19) chr21:g.44287356C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44287356C>T , CM000683.2:g.44287356C>T GRCh38
NC_000021.8:g.45707239C>T , CM000683.1:g.45707239C>T GRCh37
NC_000021.7:g.44531667C>T NCBI36
NG_009556.1:g.6477C>T , LRG_18:g.6477C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.464-161C>T MANE Select ENSP00000291582.5:n.464-161C>T
ENST00000291582.5:c.464-161C>T ENSP00000291582.5:n.464-161C>T
ENST00000527919.5:n.847C>T
ENST00000530812.5:n.855C>T
NM_000383.3:c.464-161C>T NP_000374.1:n.464-161C>T
XM_011529551.1:c.464-161C>T XP_011527853.1:n.464-161C>T
NM_000383.4:c.464-161C>T MANE Select NP_000374.1:n.464-161C>T
Search 100 bp 5'
Search 100 bp 3'