Canonical Allele Identifier: CA2326165146

Gene: IL12RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059924G= , CM000681.2:g.18059924G=	GRCh38
NC_000019.9:g.18170734G= , CM000681.1:g.18170734G=	GRCh37
NC_000019.8:g.18031734G=	NCBI36
NG_007366.2:g.44026C= , LRG_72:g.44026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1953C= MANE Select	ENSP00000472165.2:p.Ser651=
ENST00000593993.6:c.1953C=	ENSP00000472165.2:p.Ser651=
ENST00000600835.6:c.1953C=	ENSP00000470788.1:p.Ser651=
NM_001290023.1:c.1953C=	NP_001276952.1:p.Ser651=
NM_001290024.1:c.2073C=	NP_001276953.1:p.Ser691=
NM_005535.2:c.1953C=	NP_005526.1:p.Ser651=
XM_006722741.2:c.2073C=	XP_006722804.2:p.Ser691=
XM_011527966.1:c.2106C=	XP_011526268.1:p.Ser702=
XM_011527967.1:c.2094C=	XP_011526269.1:p.Ser698=
XM_011527968.1:c.2085C=	XP_011526270.1:p.Ser695=
XM_011527969.1:c.2073C=	XP_011526271.1:p.Ser691=
XM_011527970.1:c.2106C=	XP_011526272.1:p.Ser702=
XM_011527971.1:c.2106C=	XP_011526273.1:p.Ser702=
XM_011527972.1:c.2106C=	XP_011526274.1:p.Ser702=
XM_011527973.1:c.1986C=	XP_011526275.1:p.Ser662=
XM_011527974.1:c.1974C=	XP_011526276.1:p.Ser658=
XM_011527975.1:c.2073C=	XP_011526277.1:p.Ser691=
XM_006722741.3:c.2073C=	XP_006722804.2:p.Ser691=
XM_011527966.2:c.2106C=	XP_011526268.1:p.Ser702=
XM_011527967.2:c.2094C=	XP_011526269.1:p.Ser698=
XM_011527968.3:c.2085C=	XP_011526270.1:p.Ser695=
XM_011527969.2:c.2073C=	XP_011526271.1:p.Ser691=
XM_011527970.2:c.2106C=	XP_011526272.1:p.Ser702=
XM_011527971.3:c.2106C=	XP_011526273.1:p.Ser702=
XM_011527972.3:c.2106C=	XP_011526274.1:p.Ser702=
XM_011527973.2:c.1986C=	XP_011526275.1:p.Ser662=
XM_011527974.2:c.1974C=	XP_011526276.1:p.Ser658=
XM_011527975.2:c.2073C=	XP_011526277.1:p.Ser691=
XM_017026762.1:c.1371C=	XP_016882251.1:p.Ser457=
NM_001290023.2:c.1953C=	NP_001276952.1:p.Ser651=
NM_005535.3:c.1953C= MANE Select	NP_005526.1:p.Ser651=