Canonical Allele Identifier: CA2583512010
Gene: IL12RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18075755del , CM000681.2:g.18075755del GRCh38
NC_000019.9:g.18186565del , CM000681.1:g.18186565del GRCh37
NC_000019.8:g.18047565del NCBI36
NG_007366.2:g.28199del , LRG_72:g.28199del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.698del MANE Select ENSP00000472165.2:p.Pro233LeufsTer9
ENST00000322153.11:c.698del ENSP00000314425.5:p.Pro233LeufsTer9
ENST00000593993.6:c.698del ENSP00000472165.2:p.Pro233LeufsTer9
ENST00000600835.6:c.698del ENSP00000470788.1:p.Pro233LeufsTer9
NM_001290023.1:c.698del NP_001276952.1:p.Pro233LeufsTer9
NM_001290024.1:c.818del NP_001276953.1:p.Pro273LeufsTer9
NM_005535.2:c.698del NP_005526.1:p.Pro233LeufsTer9
NM_153701.2:c.698del NP_714912.1:p.Pro233LeufsTer9
XM_006722741.2:c.818del XP_006722804.2:p.Pro273LeufsTer9
XM_011527966.1:c.830del XP_011526268.1:p.Pro277LeufsTer6
XM_011527967.1:c.818del XP_011526269.1:p.Pro273LeufsTer6
XM_011527968.1:c.830del XP_011526270.1:p.Pro277LeufsTer9
XM_011527969.1:c.818del XP_011526271.1:p.Pro273LeufsTer9
XM_011527970.1:c.830del XP_011526272.1:p.Pro277LeufsTer6
XM_011527971.1:c.830del XP_011526273.1:p.Pro277LeufsTer6
XM_011527972.1:c.830del XP_011526274.1:p.Pro277LeufsTer6
XM_011527973.1:c.710del XP_011526275.1:p.Pro237LeufsTer6
XM_011527974.1:c.698del XP_011526276.1:p.Pro233LeufsTer6
XM_011527975.1:c.818del XP_011526277.1:p.Pro273LeufsTer9
XM_011527976.1:c.830del XP_011526278.1:p.Pro277LeufsTer6
XM_011527977.1:c.818del XP_011526279.1:p.Pro273LeufsTer9
XM_006722741.3:c.818del XP_006722804.2:p.Pro273LeufsTer9
XM_011527966.2:c.830del XP_011526268.1:p.Pro277LeufsTer6
XM_011527967.2:c.818del XP_011526269.1:p.Pro273LeufsTer6
XM_011527968.3:c.830del XP_011526270.1:p.Pro277LeufsTer9
XM_011527969.2:c.818del XP_011526271.1:p.Pro273LeufsTer9
XM_011527970.2:c.830del XP_011526272.1:p.Pro277LeufsTer6
XM_011527971.3:c.830del XP_011526273.1:p.Pro277LeufsTer6
XM_011527972.3:c.830del XP_011526274.1:p.Pro277LeufsTer6
XM_011527973.2:c.710del XP_011526275.1:p.Pro237LeufsTer6
XM_011527974.2:c.698del XP_011526276.1:p.Pro233LeufsTer6
XM_011527975.2:c.818del XP_011526277.1:p.Pro273LeufsTer9
XM_011527976.2:c.830del XP_011526278.1:p.Pro277LeufsTer6
XM_011527977.2:c.818del XP_011526279.1:p.Pro273LeufsTer9
XM_017026762.1:c.95del XP_016882251.1:p.Pro32LeufsTer6
NM_001290023.2:c.698del NP_001276952.1:p.Pro233LeufsTer9
NM_005535.3:c.698del MANE Select NP_005526.1:p.Pro233LeufsTer9
NM_153701.3:c.698del NP_714912.1:p.Pro233LeufsTer9