Canonical Allele Identifier: CA148217454
Gene: IL22RA2 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.137156686C>T
GRCh37 chr6:g.137477823C>T
gnomAD v2:
6:137477823 C / T
gnomAD v3:
6:137156686 C / T
gnomAD v4:
chr6-137156686-C-T
Joint Max Group AF 0.85424412 (AFR)
Genomes Max Group AF 0.84687805 (AFR)
Exomes Max Group AF 0.85844211 (AFR)
dbSNP:
2064501
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137156686C>T , CM000668.2:g.137156686C>T GRCh38
NC_000006.11:g.137477823C>T , CM000668.1:g.137477823C>T GRCh37
NC_000006.10:g.137519516C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349184.9:c.198-1567G>A ENSP00000296979.4:n.198-1567G>A
ENST00000296980.7:c.293+73G>A MANE Select ENSP00000296980.2:n.293+73G>A
ENST00000296980.6:c.293+73G>A ENSP00000296980.2:n.293+73G>A
ENST00000339602.3:c.198-1567G>A ENSP00000340920.3:n.198-1567G>A
ENST00000349184.8:c.198-1567G>A ENSP00000296979.4:n.198-1567G>A
NM_052962.2:c.293+73G>A NP_443194.1:n.293+73G>A
NM_181309.1:c.198-1567G>A NP_851826.1:n.198-1567G>A
NM_181310.1:c.198-1567G>A NP_851827.1:n.198-1567G>A
NM_052962.3:c.293+73G>A MANE Select NP_443194.1:n.293+73G>A
NM_181309.2:c.198-1567G>A NP_851826.1:n.198-1567G>A
NM_181310.2:c.198-1567G>A NP_851827.1:n.198-1567G>A
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