Canonical Allele Identifier: CA148211270
Gene: IL22RA2 HGNC NCBI

Linked Data

dbSNP Id: rs2038610

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137146963C>T , CM000668.2:g.137146963C>T GRCh38
NC_000006.11:g.137468100C>T , CM000668.1:g.137468100C>T GRCh37
NC_000006.10:g.137509793C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000349184.9:c.546+759G>A ENSP00000296979.4:n.546+759G>A
ENST00000296980.7:c.642+759G>A MANE Select ENSP00000296980.2:n.642+759G>A
ENST00000296980.6:c.642+759G>A ENSP00000296980.2:n.642+759G>A
ENST00000339602.3:c.377-1190G>A ENSP00000340920.3:n.377-1190G>A
ENST00000349184.8:c.546+759G>A ENSP00000296979.4:n.546+759G>A
NM_052962.2:c.642+759G>A NP_443194.1:n.642+759G>A
NM_181309.1:c.546+759G>A NP_851826.1:n.546+759G>A
NM_181310.1:c.377-1190G>A NP_851827.1:n.377-1190G>A
NM_052962.3:c.642+759G>A MANE Select NP_443194.1:n.642+759G>A
NM_181309.2:c.546+759G>A NP_851826.1:n.546+759G>A
NM_181310.2:c.377-1190G>A NP_851827.1:n.377-1190G>A