Canonical Allele Identifier: CA948825038
Gene: IL22 HGNC NCBI

Linked Data

dbSNP Id: rs190490002
gnomAD v3: 12-68249851-G-T
gnomAD v4: 12-68249851-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68249851G>T , CM000674.2:g.68249851G>T GRCh38
NC_000012.11:g.68643631G>T , CM000674.1:g.68643631G>T GRCh37
NC_000012.10:g.66929898G>T NCBI36
NG_060763.1:g.8754C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-975C>A ENSP00000329384.4:n.463-975C>A
ENST00000538666.6:c.463-975C>A MANE Select ENSP00000442424.1:n.463-975C>A
ENST00000328087.5:c.463-975C>A ENSP00000329384.4:n.463-975C>A
ENST00000538666.5:c.463-975C>A ENSP00000442424.1:n.463-975C>A
NM_020525.4:c.463-975C>A NP_065386.1:n.463-975C>A
XR_945055.1:n.265-14807G>T
NM_020525.5:c.463-975C>A MANE Select NP_065386.1:n.463-975C>A
XR_002957418.1:n.281-14807G>T
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