Canonical Allele Identifier: CA238383575
Gene: IL22 HGNC NCBI

Linked Data

dbSNP Id: rs917993831
gnomAD v2: 12-68643575-C-T
gnomAD v3: 12-68249795-C-T
gnomAD v4: 12-68249795-C-T
MyVariant Identifiers: chr12:g.68643575C>T (hg19) chr12:g.68249795C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68249795C>T , CM000674.2:g.68249795C>T GRCh38
NC_000012.11:g.68643575C>T , CM000674.1:g.68643575C>T GRCh37
NC_000012.10:g.66929842C>T NCBI36
NG_060763.1:g.8810G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-919G>A ENSP00000329384.4:n.463-919G>A
ENST00000538666.6:c.463-919G>A MANE Select ENSP00000442424.1:n.463-919G>A
ENST00000328087.5:c.463-919G>A ENSP00000329384.4:n.463-919G>A
ENST00000538666.5:c.463-919G>A ENSP00000442424.1:n.463-919G>A
NM_020525.4:c.463-919G>A NP_065386.1:n.463-919G>A
XR_945055.1:n.265-14863C>T
NM_020525.5:c.463-919G>A MANE Select NP_065386.1:n.463-919G>A
XR_002957418.1:n.281-14863C>T
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