Canonical Allele Identifier: CA2326172926

Gene: IL12RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18075813T= , CM000681.2:g.18075813T=	GRCh38
NC_000019.9:g.18186623T= , CM000681.1:g.18186623T=	GRCh37
NC_000019.8:g.18047623T=	NCBI36
NG_007366.2:g.28137A= , LRG_72:g.28137A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000593993.7:c.636A= MANE Select	ENSP00000472165.2:p.Arg212=
ENST00000322153.11:c.636A=	ENSP00000314425.5:p.Arg212=
ENST00000593993.6:c.636A=	ENSP00000472165.2:p.Arg212=
ENST00000600835.6:c.636A=	ENSP00000470788.1:p.Arg212=
NM_001290023.1:c.636A=	NP_001276952.1:p.Arg212=
NM_001290024.1:c.756A=	NP_001276953.1:p.Arg252=
NM_005535.2:c.636A=	NP_005526.1:p.Arg212=
NM_153701.2:c.636A=	NP_714912.1:p.Arg212=
XM_006722741.2:c.756A=	XP_006722804.2:p.Arg252=
XM_011527966.1:c.768A=	XP_011526268.1:p.Arg256=
XM_011527967.1:c.756A=	XP_011526269.1:p.Arg252=
XM_011527968.1:c.768A=	XP_011526270.1:p.Arg256=
XM_011527969.1:c.756A=	XP_011526271.1:p.Arg252=
XM_011527970.1:c.768A=	XP_011526272.1:p.Arg256=
XM_011527971.1:c.768A=	XP_011526273.1:p.Arg256=
XM_011527972.1:c.768A=	XP_011526274.1:p.Arg256=
XM_011527973.1:c.648A=	XP_011526275.1:p.Arg216=
XM_011527974.1:c.636A=	XP_011526276.1:p.Arg212=
XM_011527975.1:c.756A=	XP_011526277.1:p.Arg252=
XM_011527976.1:c.768A=	XP_011526278.1:p.Arg256=
XM_011527977.1:c.756A=	XP_011526279.1:p.Arg252=
XM_006722741.3:c.756A=	XP_006722804.2:p.Arg252=
XM_011527966.2:c.768A=	XP_011526268.1:p.Arg256=
XM_011527967.2:c.756A=	XP_011526269.1:p.Arg252=
XM_011527968.3:c.768A=	XP_011526270.1:p.Arg256=
XM_011527969.2:c.756A=	XP_011526271.1:p.Arg252=
XM_011527970.2:c.768A=	XP_011526272.1:p.Arg256=
XM_011527971.3:c.768A=	XP_011526273.1:p.Arg256=
XM_011527972.3:c.768A=	XP_011526274.1:p.Arg256=
XM_011527973.2:c.648A=	XP_011526275.1:p.Arg216=
XM_011527974.2:c.636A=	XP_011526276.1:p.Arg212=
XM_011527975.2:c.756A=	XP_011526277.1:p.Arg252=
XM_011527976.2:c.768A=	XP_011526278.1:p.Arg256=
XM_011527977.2:c.756A=	XP_011526279.1:p.Arg252=
XM_017026762.1:c.33A=	XP_016882251.1:p.Arg11=
NM_001290023.2:c.636A=	NP_001276952.1:p.Arg212=
NM_005535.3:c.636A= MANE Select	NP_005526.1:p.Arg212=
NM_153701.3:c.636A=	NP_714912.1:p.Arg212=