Canonical Allele Identifier: CA638115837
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs1178929417
gnomAD v2: 21-45708676-C-T
gnomAD v3: 21-44288793-C-T
gnomAD v4: 21-44288793-C-T
MyVariant Identifiers: chr21:g.45708676C>T (hg19) chr21:g.44288793C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44288793C>T , CM000683.2:g.44288793C>T GRCh38
NC_000021.8:g.45708676C>T , CM000683.1:g.45708676C>T GRCh37
NC_000021.7:g.44533104C>T NCBI36
NG_009556.1:g.7914C>T , LRG_18:g.7914C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.652+335C>T MANE Select ENSP00000291582.5:n.652+335C>T
ENST00000291582.5:c.652+335C>T ENSP00000291582.5:n.652+335C>T
ENST00000527919.5:n.1196+335C>T
ENST00000530812.5:n.1539C>T
NM_000383.3:c.652+335C>T NP_000374.1:n.652+335C>T
XM_011529551.1:c.652+335C>T XP_011527853.1:n.652+335C>T
NM_000383.4:c.652+335C>T MANE Select NP_000374.1:n.652+335C>T
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