Canonical Allele Identifier: CA819508108
Gene: IL22RA2 HGNC NCBI

Linked Data

dbSNP Id: rs2064501
gnomAD v4: 6-137156686-C-G
MyVariant Identifiers: chr6:g.137477823C>G (hg19) chr6:g.137156686C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137156686C>G , CM000668.2:g.137156686C>G GRCh38
NC_000006.11:g.137477823C>G , CM000668.1:g.137477823C>G GRCh37
NC_000006.10:g.137519516C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000349184.9:c.198-1567G>C ENSP00000296979.4:n.198-1567G>C
ENST00000296980.7:c.293+73G>C MANE Select ENSP00000296980.2:n.293+73G>C
ENST00000296980.6:c.293+73G>C ENSP00000296980.2:n.293+73G>C
ENST00000339602.3:c.198-1567G>C ENSP00000340920.3:n.198-1567G>C
ENST00000349184.8:c.198-1567G>C ENSP00000296979.4:n.198-1567G>C
NM_052962.2:c.293+73G>C NP_443194.1:n.293+73G>C
NM_181309.1:c.198-1567G>C NP_851826.1:n.198-1567G>C
NM_181310.1:c.198-1567G>C NP_851827.1:n.198-1567G>C
NM_052962.3:c.293+73G>C MANE Select NP_443194.1:n.293+73G>C
NM_181309.2:c.198-1567G>C NP_851826.1:n.198-1567G>C
NM_181310.2:c.198-1567G>C NP_851827.1:n.198-1567G>C
Search 100 bp 5'
Search 100 bp 3'