Canonical Allele Identifier: CA2043865024
Gene: IL22 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68250026C= , CM000674.2:g.68250026C= GRCh38
NC_000012.11:g.68643806C= , CM000674.1:g.68643806C= GRCh37
NC_000012.10:g.66930073C= NCBI36
NG_060763.1:g.8579G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-1150G= ENSP00000329384.4:n.463-1150G=
ENST00000538666.6:c.463-1150G= MANE Select ENSP00000442424.1:n.463-1150G=
ENST00000328087.5:c.463-1150G= ENSP00000329384.4:n.463-1150G=
ENST00000538666.5:c.463-1150G= ENSP00000442424.1:n.463-1150G=
NM_020525.4:c.463-1150G= NP_065386.1:n.463-1150G=
XR_945055.1:n.265-14632C=
NM_020525.5:c.463-1150G= MANE Select NP_065386.1:n.463-1150G=
XR_002957418.1:n.281-14632C=
Search 100 bp 5'
Search 100 bp 3'