Canonical Allele Identifier: CA238383626

Gene: IL22

Linked Data

• dbSNP Id: rs890815221
• MyVariant Identifiers: chr12:g.68249871T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68249871T>C , CM000674.2:g.68249871T>C	GRCh38
NC_000012.11:g.68643651T>C , CM000674.1:g.68643651T>C	GRCh37
NC_000012.10:g.66929918T>C	NCBI36
NG_060763.1:g.8734A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328087.6:c.463-995A>G	ENSP00000329384.4:n.463-995A>G
ENST00000538666.6:c.463-995A>G MANE Select	ENSP00000442424.1:n.463-995A>G
ENST00000328087.5:c.463-995A>G	ENSP00000329384.4:n.463-995A>G
ENST00000538666.5:c.463-995A>G	ENSP00000442424.1:n.463-995A>G
NM_020525.4:c.463-995A>G	NP_065386.1:n.463-995A>G
XR_945055.1:n.265-14787T>C
NM_020525.5:c.463-995A>G MANE Select	NP_065386.1:n.463-995A>G
XR_002957418.1:n.281-14787T>C