Canonical Allele Identifier: CA6676254
Gene: IL22 HGNC NCBI
COSMIC:
COSN17153822 (not active)
MyVariant.info:
GRCh38 chr12:g.68252741T>C
GRCh37 chr12:g.68646521T>C
gnomAD v2:
12:68646521 T / C
gnomAD v3:
12:68252741 T / C
gnomAD v4:
chr12-68252741-T-C
Joint Max Group AF 0.62808643 (AFR)
Genomes Max Group AF 0.62853675 (AFR)
Exomes Max Group AF 0.62313251 (AFR)
dbSNP:
2227491
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68252741T>C , CM000674.2:g.68252741T>C GRCh38
NC_000012.11:g.68646521T>C , CM000674.1:g.68646521T>C GRCh37
NC_000012.10:g.66932788T>C NCBI36
NG_060763.1:g.5864A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.252+23A>G ENSP00000329384.4:n.252+23A>G
ENST00000538666.6:c.252+23A>G MANE Select ENSP00000442424.1:n.252+23A>G
ENST00000328087.5:c.252+23A>G ENSP00000329384.4:n.252+23A>G
ENST00000538666.5:c.252+23A>G ENSP00000442424.1:n.252+23A>G
NM_020525.4:c.252+23A>G NP_065386.1:n.252+23A>G
XR_945055.1:n.265-11917T>C
NM_020525.5:c.252+23A>G MANE Select NP_065386.1:n.252+23A>G
XR_002957418.1:n.281-11917T>C
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