Canonical Allele Identifier: CA2598559155
Gene: IL22 HGNC NCBI

Linked Data

gnomAD v3: 12-68250120-C-A
gnomAD v4: 12-68250120-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68250120C>A , CM000674.2:g.68250120C>A GRCh38
NC_000012.11:g.68643900C>A , CM000674.1:g.68643900C>A GRCh37
NC_000012.10:g.66930167C>A NCBI36
NG_060763.1:g.8485G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-1244G>T ENSP00000329384.4:n.463-1244G>T
ENST00000538666.6:c.463-1244G>T MANE Select ENSP00000442424.1:n.463-1244G>T
ENST00000328087.5:c.463-1244G>T ENSP00000329384.4:n.463-1244G>T
ENST00000538666.5:c.463-1244G>T ENSP00000442424.1:n.463-1244G>T
NM_020525.4:c.463-1244G>T NP_065386.1:n.463-1244G>T
XR_945055.1:n.265-14538C>A
NM_020525.5:c.463-1244G>T MANE Select NP_065386.1:n.463-1244G>T
XR_002957418.1:n.281-14538C>A
Search 100 bp 5'
Search 100 bp 3'