Canonical Allele Identifier: CA238383899
Gene: IL22 HGNC NCBI

Linked Data

dbSNP Id: rs964470208
MyVariant Identifiers: chr12:g.68644008G>A (hg19) chr12:g.68250228G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68250228G>A , CM000674.2:g.68250228G>A GRCh38
NC_000012.11:g.68644008G>A , CM000674.1:g.68644008G>A GRCh37
NC_000012.10:g.66930275G>A NCBI36
NG_060763.1:g.8377C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.462+1285C>T ENSP00000329384.4:n.462+1285C>T
ENST00000538666.6:c.462+1285C>T MANE Select ENSP00000442424.1:n.462+1285C>T
ENST00000328087.5:c.462+1285C>T ENSP00000329384.4:n.462+1285C>T
ENST00000538666.5:c.462+1285C>T ENSP00000442424.1:n.462+1285C>T
NM_020525.4:c.462+1285C>T NP_065386.1:n.462+1285C>T
XR_945055.1:n.265-14430G>A
NM_020525.5:c.462+1285C>T MANE Select NP_065386.1:n.462+1285C>T
XR_002957418.1:n.281-14430G>A
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