Canonical Allele Identifier: CA2043865099
Gene: IL22 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68250228G= , CM000674.2:g.68250228G= GRCh38
NC_000012.11:g.68644008G= , CM000674.1:g.68644008G= GRCh37
NC_000012.10:g.66930275G= NCBI36
NG_060763.1:g.8377C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.462+1285C= ENSP00000329384.4:n.462+1285C=
ENST00000538666.6:c.462+1285C= MANE Select ENSP00000442424.1:n.462+1285C=
ENST00000328087.5:c.462+1285C= ENSP00000329384.4:n.462+1285C=
ENST00000538666.5:c.462+1285C= ENSP00000442424.1:n.462+1285C=
NM_020525.4:c.462+1285C= NP_065386.1:n.462+1285C=
XR_945055.1:n.265-14430G=
NM_020525.5:c.462+1285C= MANE Select NP_065386.1:n.462+1285C=
XR_002957418.1:n.281-14430G=
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