Canonical Allele Identifier: CA354658237
Gene: IL20RB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.137010114A>T , CM000665.2:g.137010114A>T GRCh38
NC_000003.11:g.136728956A>T , CM000665.1:g.136728956A>T GRCh37
NC_000003.10:g.138211646A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_144717.4:c.827A>T MANE Select NP_653318.2:p.Lys276Ile
ENST00000329582.9:c.827A>T MANE Select ENSP00000328133.4:p.Lys276Ile
NM_144717.3:c.827A>T NP_653318.2:p.Lys276Ile
ENST00000329582.8:c.827A>T ENSP00000328133.4:p.Lys276Ile
ENST00000469964.5:c.*661A>T ENSP00000418637.1:n.*661A>T
ENST00000475972.1:c.822A>T ENSP00000420725.1:n.822A>T
XM_006713665.2:c.686A>T XP_006713728.1:p.Lys229Ile
XM_006713665.4:c.686A>T XP_006713728.1:p.Lys229Ile
XM_011512910.1:c.842A>T XP_011511212.1:p.Lys281Ile
XM_011512910.3:c.842A>T XP_011511212.1:p.Lys281Ile
XM_011512911.1:c.686A>T XP_011511213.1:p.Lys229Ile
XM_011512911.2:c.686A>T XP_011511213.1:p.Lys229Ile
XM_017006632.1:c.686A>T XP_016862121.1:p.Lys229Ile