Canonical Allele Identifier: CA15769853
Gene: IL22 HGNC NCBI

Linked Data

dbSNP Id: rs2227501

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68250179G>T , CM000674.2:g.68250179G>T GRCh38
NC_000012.11:g.68643959G>T , CM000674.1:g.68643959G>T GRCh37
NC_000012.10:g.66930226G>T NCBI36
NG_060763.1:g.8426C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000328087.6:c.463-1303C>A ENSP00000329384.4:n.463-1303C>A
ENST00000538666.6:c.463-1303C>A MANE Select ENSP00000442424.1:n.463-1303C>A
ENST00000328087.5:c.463-1303C>A ENSP00000329384.4:n.463-1303C>A
ENST00000538666.5:c.463-1303C>A ENSP00000442424.1:n.463-1303C>A
NM_020525.4:c.463-1303C>A NP_065386.1:n.463-1303C>A
XR_945055.1:n.265-14479G>T
NM_020525.5:c.463-1303C>A MANE Select NP_065386.1:n.463-1303C>A
XR_002957418.1:n.281-14479G>T