Canonical Allele Identifier: CA2326165197

Gene: IL12RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18060030G= , CM000681.2:g.18060030G=	GRCh38
NC_000019.9:g.18170840G= , CM000681.1:g.18170840G=	GRCh37
NC_000019.8:g.18031840G=	NCBI36
NG_007366.2:g.43920C= , LRG_72:g.43920C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1847C= MANE Select	ENSP00000472165.2:p.Ala616=
ENST00000593993.6:c.1847C=	ENSP00000472165.2:p.Ala616=
ENST00000600835.6:c.1847C=	ENSP00000470788.1:p.Ala616=
NM_001290023.1:c.1847C=	NP_001276952.1:p.Ala616=
NM_001290024.1:c.1967C=	NP_001276953.1:p.Ala656=
NM_005535.2:c.1847C=	NP_005526.1:p.Ala616=
XM_006722741.2:c.1967C=	XP_006722804.2:p.Ala656=
XM_011527966.1:c.2000C=	XP_011526268.1:p.Ala667=
XM_011527967.1:c.1988C=	XP_011526269.1:p.Ala663=
XM_011527968.1:c.1979C=	XP_011526270.1:p.Ala660=
XM_011527969.1:c.1967C=	XP_011526271.1:p.Ala656=
XM_011527970.1:c.2000C=	XP_011526272.1:p.Ala667=
XM_011527971.1:c.2000C=	XP_011526273.1:p.Ala667=
XM_011527972.1:c.2000C=	XP_011526274.1:p.Ala667=
XM_011527973.1:c.1880C=	XP_011526275.1:p.Ala627=
XM_011527974.1:c.1868C=	XP_011526276.1:p.Ala623=
XM_011527975.1:c.1967C=	XP_011526277.1:p.Ala656=
XM_006722741.3:c.1967C=	XP_006722804.2:p.Ala656=
XM_011527966.2:c.2000C=	XP_011526268.1:p.Ala667=
XM_011527967.2:c.1988C=	XP_011526269.1:p.Ala663=
XM_011527968.3:c.1979C=	XP_011526270.1:p.Ala660=
XM_011527969.2:c.1967C=	XP_011526271.1:p.Ala656=
XM_011527970.2:c.2000C=	XP_011526272.1:p.Ala667=
XM_011527971.3:c.2000C=	XP_011526273.1:p.Ala667=
XM_011527972.3:c.2000C=	XP_011526274.1:p.Ala667=
XM_011527973.2:c.1880C=	XP_011526275.1:p.Ala627=
XM_011527974.2:c.1868C=	XP_011526276.1:p.Ala623=
XM_011527975.2:c.1967C=	XP_011526277.1:p.Ala656=
XM_017026762.1:c.1265C=	XP_016882251.1:p.Ala422=
NM_001290023.2:c.1847C=	NP_001276952.1:p.Ala616=
NM_005535.3:c.1847C= MANE Select	NP_005526.1:p.Ala616=