Canonical Allele Identifier: CA2043864969

Gene: IL22

Linked Data

• dbSNP Id: rs1869870376

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68249936_68249938del , CM000674.2:g.68249936_68249938del	GRCh38
NC_000012.11:g.68643716_68643718del , CM000674.1:g.68643716_68643718del	GRCh37
NC_000012.10:g.66929983_66929985del	NCBI36
NG_060763.1:g.8668_8670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328087.6:c.463-1061_463-1059del	ENSP00000329384.4:n.463-1061_463-1059del
ENST00000538666.6:c.463-1061_463-1059del MANE Select	ENSP00000442424.1:n.463-1061_463-1059del
ENST00000328087.5:c.463-1061_463-1059del	ENSP00000329384.4:n.463-1061_463-1059del
ENST00000538666.5:c.463-1061_463-1059del	ENSP00000442424.1:n.463-1061_463-1059del
NM_020525.4:c.463-1061_463-1059del	NP_065386.1:n.463-1061_463-1059del
XR_945055.1:n.265-14722_265-14720del
NM_020525.5:c.463-1061_463-1059del MANE Select	NP_065386.1:n.463-1061_463-1059del
XR_002957418.1:n.281-14722_281-14720del