Canonical Allele Identifier: CA321788568
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs1039024362
gnomAD v4: 21-44288774-C-T
MyVariant Identifiers: chr21:g.45708657C>T (hg19) chr21:g.44288774C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44288774C>T , CM000683.2:g.44288774C>T GRCh38
NC_000021.8:g.45708657C>T , CM000683.1:g.45708657C>T GRCh37
NC_000021.7:g.44533085C>T NCBI36
NG_009556.1:g.7895C>T , LRG_18:g.7895C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.652+316C>T MANE Select ENSP00000291582.5:n.652+316C>T
ENST00000291582.5:c.652+316C>T ENSP00000291582.5:n.652+316C>T
ENST00000527919.5:n.1196+316C>T
ENST00000530812.5:n.1520C>T
NM_000383.3:c.652+316C>T NP_000374.1:n.652+316C>T
XM_011529551.1:c.652+316C>T XP_011527853.1:n.652+316C>T
NM_000383.4:c.652+316C>T MANE Select NP_000374.1:n.652+316C>T
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