Canonical Allele Identifier: CA506026123

Gene: IL12RB1

Linked Data

• MyVariant Identifiers: chr19:g.18170805T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059995T>G , CM000681.2:g.18059995T>G	GRCh38
NC_000019.9:g.18170805T>G , CM000681.1:g.18170805T>G	GRCh37
NC_000019.8:g.18031805T>G	NCBI36
NG_007366.2:g.43955A>C , LRG_72:g.43955A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1882A>C MANE Select	ENSP00000472165.2:p.Arg628=
ENST00000593993.6:c.1882A>C	ENSP00000472165.2:p.Arg628=
ENST00000600835.6:c.1882A>C	ENSP00000470788.1:p.Arg628=
NM_001290023.1:c.1882A>C	NP_001276952.1:p.Arg628=
NM_001290024.1:c.2002A>C	NP_001276953.1:p.Arg668=
NM_005535.2:c.1882A>C	NP_005526.1:p.Arg628=
XM_006722741.2:c.2002A>C	XP_006722804.2:p.Arg668=
XM_011527966.1:c.2035A>C	XP_011526268.1:p.Arg679=
XM_011527967.1:c.2023A>C	XP_011526269.1:p.Arg675=
XM_011527968.1:c.2014A>C	XP_011526270.1:p.Arg672=
XM_011527969.1:c.2002A>C	XP_011526271.1:p.Arg668=
XM_011527970.1:c.2035A>C	XP_011526272.1:p.Arg679=
XM_011527971.1:c.2035A>C	XP_011526273.1:p.Arg679=
XM_011527972.1:c.2035A>C	XP_011526274.1:p.Arg679=
XM_011527973.1:c.1915A>C	XP_011526275.1:p.Arg639=
XM_011527974.1:c.1903A>C	XP_011526276.1:p.Arg635=
XM_011527975.1:c.2002A>C	XP_011526277.1:p.Arg668=
XM_006722741.3:c.2002A>C	XP_006722804.2:p.Arg668=
XM_011527966.2:c.2035A>C	XP_011526268.1:p.Arg679=
XM_011527967.2:c.2023A>C	XP_011526269.1:p.Arg675=
XM_011527968.3:c.2014A>C	XP_011526270.1:p.Arg672=
XM_011527969.2:c.2002A>C	XP_011526271.1:p.Arg668=
XM_011527970.2:c.2035A>C	XP_011526272.1:p.Arg679=
XM_011527971.3:c.2035A>C	XP_011526273.1:p.Arg679=
XM_011527972.3:c.2035A>C	XP_011526274.1:p.Arg679=
XM_011527973.2:c.1915A>C	XP_011526275.1:p.Arg639=
XM_011527974.2:c.1903A>C	XP_011526276.1:p.Arg635=
XM_011527975.2:c.2002A>C	XP_011526277.1:p.Arg668=
XM_017026762.1:c.1300A>C	XP_016882251.1:p.Arg434=
NM_001290023.2:c.1882A>C	NP_001276952.1:p.Arg628=
NM_005535.3:c.1882A>C MANE Select	NP_005526.1:p.Arg628=