Canonical Allele Identifier: CA2043864921
Gene: IL22 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68249855T= , CM000674.2:g.68249855T= GRCh38
NC_000012.11:g.68643635T= , CM000674.1:g.68643635T= GRCh37
NC_000012.10:g.66929902T= NCBI36
NG_060763.1:g.8750A=

Transcript Alleles

HGVS Amino-acid change
ENST00000328087.6:c.463-979A= ENSP00000329384.4:n.463-979A=
ENST00000538666.6:c.463-979A= MANE Select ENSP00000442424.1:n.463-979A=
ENST00000328087.5:c.463-979A= ENSP00000329384.4:n.463-979A=
ENST00000538666.5:c.463-979A= ENSP00000442424.1:n.463-979A=
NM_020525.4:c.463-979A= NP_065386.1:n.463-979A=
XR_945055.1:n.265-14803T=
NM_020525.5:c.463-979A= MANE Select NP_065386.1:n.463-979A=
XR_002957418.1:n.281-14803T=
Search 100 bp 5'
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