Canonical Allele Identifier: CA10051506
Gene: AIRE HGNC NCBI

Linked Data

dbSNP Id: rs762267080
ExAC: 21:45706573 G / C
gnomAD v2: 21-45706573-G-C
MyVariant Identifiers: chr21:g.45706573G>C (hg19) chr21:g.44286690G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44286690G>C , CM000683.2:g.44286690G>C GRCh38
NC_000021.8:g.45706573G>C , CM000683.1:g.45706573G>C GRCh37
NC_000021.7:g.44531001G>C NCBI36
NG_009556.1:g.5811G>C , LRG_18:g.5811G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000291582.6:c.266G>C MANE Select ENSP00000291582.5:p.Arg89Pro
ENST00000291582.5:c.266G>C ENSP00000291582.5:p.Arg89Pro
ENST00000527919.5:n.427G>C
ENST00000530812.5:n.435G>C
NM_000383.3:c.266G>C NP_000374.1:p.Arg89Pro
XM_011529551.1:c.266G>C XP_011527853.1:p.Arg89Pro
NM_000383.4:c.266G>C MANE Select NP_000374.1:p.Arg89Pro
Search 100 bp 5'
Search 100 bp 3'