Canonical Allele Identifier: CA512490721
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs2146377797
MyVariant Identifiers: chr21:g.45708280G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44288397G>A , CM000683.2:g.44288397G>A GRCh38
NC_000021.8:g.45708280G>A , CM000683.1:g.45708280G>A GRCh37
NC_000021.7:g.44532708G>A NCBI36
NG_009556.1:g.7518G>A , LRG_18:g.7518G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000291582.6:c.591G>A MANE Select ENSP00000291582.5:p.Gly197=
ENST00000291582.5:c.591G>A ENSP00000291582.5:p.Gly197=
ENST00000527919.5:n.1135G>A
ENST00000530812.5:n.1143G>A
NM_000383.3:c.591G>A NP_000374.1:p.Gly197=
XM_011529551.1:c.591G>A XP_011527853.1:p.Gly197=
NM_000383.4:c.591G>A MANE Select NP_000374.1:p.Gly197=
Search 100 bp 5'
Search 100 bp 3'