Canonical Allele Identifier: CA2576772386
Gene: IL12RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18069751del , CM000681.2:g.18069751del GRCh38
NC_000019.9:g.18180561del , CM000681.1:g.18180561del GRCh37
NC_000019.8:g.18041561del NCBI36
NG_007366.2:g.34200del , LRG_72:g.34200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593993.7:c.1022-37del MANE Select ENSP00000472165.2:n.1022-37del
ENST00000593993.6:c.1022-37del ENSP00000472165.2:n.1022-37del
ENST00000600835.6:c.1022-37del ENSP00000470788.1:n.1022-37del
NM_001290023.1:c.1022-37del NP_001276952.1:n.1022-37del
NM_001290024.1:c.1142-37del NP_001276953.1:n.1142-37del
NM_005535.2:c.1022-37del NP_005526.1:n.1022-37del
XM_006722741.2:c.1142-37del XP_006722804.2:n.1142-37del
XM_011527966.1:c.1175-37del XP_011526268.1:n.1175-37del
XM_011527967.1:c.1163-37del XP_011526269.1:n.1163-37del
XM_011527968.1:c.1154-37del XP_011526270.1:n.1154-37del
XM_011527969.1:c.1142-37del XP_011526271.1:n.1142-37del
XM_011527970.1:c.1175-37del XP_011526272.1:n.1175-37del
XM_011527971.1:c.1175-37del XP_011526273.1:n.1175-37del
XM_011527972.1:c.1175-37del XP_011526274.1:n.1175-37del
XM_011527973.1:c.1055-37del XP_011526275.1:n.1055-37del
XM_011527974.1:c.1043-37del XP_011526276.1:n.1043-37del
XM_011527975.1:c.1142-37del XP_011526277.1:n.1142-37del
XM_011527976.1:c.1175-37del XP_011526278.1:n.1175-37del
XM_006722741.3:c.1142-37del XP_006722804.2:n.1142-37del
XM_011527966.2:c.1175-37del XP_011526268.1:n.1175-37del
XM_011527967.2:c.1163-37del XP_011526269.1:n.1163-37del
XM_011527968.3:c.1154-37del XP_011526270.1:n.1154-37del
XM_011527969.2:c.1142-37del XP_011526271.1:n.1142-37del
XM_011527970.2:c.1175-37del XP_011526272.1:n.1175-37del
XM_011527971.3:c.1175-37del XP_011526273.1:n.1175-37del
XM_011527972.3:c.1175-37del XP_011526274.1:n.1175-37del
XM_011527973.2:c.1055-37del XP_011526275.1:n.1055-37del
XM_011527974.2:c.1043-37del XP_011526276.1:n.1043-37del
XM_011527975.2:c.1142-37del XP_011526277.1:n.1142-37del
XM_011527976.2:c.1175-37del XP_011526278.1:n.1175-37del
XM_017026762.1:c.440-37del XP_016882251.1:n.440-37del
NM_001290023.2:c.1022-37del NP_001276952.1:n.1022-37del
NM_005535.3:c.1022-37del MANE Select NP_005526.1:n.1022-37del