Canonical Allele Identifier: CA2326165137

Gene: IL12RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059907C= , CM000681.2:g.18059907C=	GRCh38
NC_000019.9:g.18170717C= , CM000681.1:g.18170717C=	GRCh37
NC_000019.8:g.18031717C=	NCBI36
NG_007366.2:g.44043G= , LRG_72:g.44043G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1970G= MANE Select	ENSP00000472165.2:p.Arg657=
ENST00000593993.6:c.1970G=	ENSP00000472165.2:p.Arg657=
ENST00000600835.6:c.1970G=	ENSP00000470788.1:p.Arg657=
NM_001290023.1:c.1970G=	NP_001276952.1:p.Arg657=
NM_001290024.1:c.2090G=	NP_001276953.1:p.Arg697=
NM_005535.2:c.1970G=	NP_005526.1:p.Arg657=
XM_006722741.2:c.2090G=	XP_006722804.2:p.Arg697=
XM_011527966.1:c.2123G=	XP_011526268.1:p.Arg708=
XM_011527967.1:c.2111G=	XP_011526269.1:p.Arg704=
XM_011527968.1:c.2102G=	XP_011526270.1:p.Arg701=
XM_011527969.1:c.2090G=	XP_011526271.1:p.Arg697=
XM_011527970.1:c.2123G=	XP_011526272.1:p.Arg708=
XM_011527971.1:c.2123G=	XP_011526273.1:p.Arg708=
XM_011527972.1:c.2123G=	XP_011526274.1:p.Arg708=
XM_011527973.1:c.2003G=	XP_011526275.1:p.Arg668=
XM_011527974.1:c.1991G=	XP_011526276.1:p.Arg664=
XM_011527975.1:c.2090G=	XP_011526277.1:p.Arg697=
XM_006722741.3:c.2090G=	XP_006722804.2:p.Arg697=
XM_011527966.2:c.2123G=	XP_011526268.1:p.Arg708=
XM_011527967.2:c.2111G=	XP_011526269.1:p.Arg704=
XM_011527968.3:c.2102G=	XP_011526270.1:p.Arg701=
XM_011527969.2:c.2090G=	XP_011526271.1:p.Arg697=
XM_011527970.2:c.2123G=	XP_011526272.1:p.Arg708=
XM_011527971.3:c.2123G=	XP_011526273.1:p.Arg708=
XM_011527972.3:c.2123G=	XP_011526274.1:p.Arg708=
XM_011527973.2:c.2003G=	XP_011526275.1:p.Arg668=
XM_011527974.2:c.1991G=	XP_011526276.1:p.Arg664=
XM_011527975.2:c.2090G=	XP_011526277.1:p.Arg697=
XM_017026762.1:c.1388G=	XP_016882251.1:p.Arg463=
NM_001290023.2:c.1970G=	NP_001276952.1:p.Arg657=
NM_005535.3:c.1970G= MANE Select	NP_005526.1:p.Arg657=