Canonical Allele Identifier: CA655165629
Gene: IL22 HGNC NCBI

Linked Data

COSMIC: COSN16218684
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68249758C>G , CM000674.2:g.68249758C>G GRCh38
NC_000012.11:g.68643538C>G , CM000674.1:g.68643538C>G GRCh37
NC_000012.10:g.66929805C>G NCBI36
NG_060763.1:g.8847G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-882G>C ENSP00000329384.4:n.463-882G>C
ENST00000538666.6:c.463-882G>C MANE Select ENSP00000442424.1:n.463-882G>C
ENST00000328087.5:c.463-882G>C ENSP00000329384.4:n.463-882G>C
ENST00000538666.5:c.463-882G>C ENSP00000442424.1:n.463-882G>C
NM_020525.4:c.463-882G>C NP_065386.1:n.463-882G>C
XR_945055.1:n.265-14900C>G
NM_020525.5:c.463-882G>C MANE Select NP_065386.1:n.463-882G>C
XR_002957418.1:n.281-14900C>G
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