Canonical Allele Identifier: CA2326169807

Gene: IL12RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18069524G= , CM000681.2:g.18069524G=	GRCh38
NC_000019.9:g.18180334G= , CM000681.1:g.18180334G=	GRCh37
NC_000019.8:g.18041334G=	NCBI36
NG_007366.2:g.34426C= , LRG_72:g.34426C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1189+22C= MANE Select	ENSP00000472165.2:n.1189+22C=
ENST00000593993.6:c.1189+22C=	ENSP00000472165.2:n.1189+22C=
ENST00000600835.6:c.1189+22C=	ENSP00000470788.1:n.1189+22C=
NM_001290023.1:c.1189+22C=	NP_001276952.1:n.1189+22C=
NM_001290024.1:c.1309+22C=	NP_001276953.1:n.1309+22C=
NM_005535.2:c.1189+22C=	NP_005526.1:n.1189+22C=
XM_006722741.2:c.1309+22C=	XP_006722804.2:n.1309+22C=
XM_011527966.1:c.1342+22C=	XP_011526268.1:n.1342+22C=
XM_011527967.1:c.1330+22C=	XP_011526269.1:n.1330+22C=
XM_011527968.1:c.1321+22C=	XP_011526270.1:n.1321+22C=
XM_011527969.1:c.1309+22C=	XP_011526271.1:n.1309+22C=
XM_011527970.1:c.1342+22C=	XP_011526272.1:n.1342+22C=
XM_011527971.1:c.1342+22C=	XP_011526273.1:n.1342+22C=
XM_011527972.1:c.1342+22C=	XP_011526274.1:n.1342+22C=
XM_011527973.1:c.1222+22C=	XP_011526275.1:n.1222+22C=
XM_011527974.1:c.1210+22C=	XP_011526276.1:n.1210+22C=
XM_011527975.1:c.1309+22C=	XP_011526277.1:n.1309+22C=
XM_011527976.1:c.1342+22C=	XP_011526278.1:n.1342+22C=
XM_006722741.3:c.1309+22C=	XP_006722804.2:n.1309+22C=
XM_011527966.2:c.1342+22C=	XP_011526268.1:n.1342+22C=
XM_011527967.2:c.1330+22C=	XP_011526269.1:n.1330+22C=
XM_011527968.3:c.1321+22C=	XP_011526270.1:n.1321+22C=
XM_011527969.2:c.1309+22C=	XP_011526271.1:n.1309+22C=
XM_011527970.2:c.1342+22C=	XP_011526272.1:n.1342+22C=
XM_011527971.3:c.1342+22C=	XP_011526273.1:n.1342+22C=
XM_011527972.3:c.1342+22C=	XP_011526274.1:n.1342+22C=
XM_011527973.2:c.1222+22C=	XP_011526275.1:n.1222+22C=
XM_011527974.2:c.1210+22C=	XP_011526276.1:n.1210+22C=
XM_011527975.2:c.1309+22C=	XP_011526277.1:n.1309+22C=
XM_011527976.2:c.1342+22C=	XP_011526278.1:n.1342+22C=
XM_017026762.1:c.607+22C=	XP_016882251.1:n.607+22C=
NM_001290023.2:c.1189+22C=	NP_001276952.1:n.1189+22C=
NM_005535.3:c.1189+22C= MANE Select	NP_005526.1:n.1189+22C=