Canonical Allele Identifier: CA506026333

Gene: IL12RB1

Linked Data

• dbSNP Id: rs1211891357
• gnomAD v2: 19-18170854-T-C
• gnomAD v4: 19-18060044-T-C
• MyVariant Identifiers: chr19:g.18170854T>C (hg19) ; chr19:g.18060044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18060044T>C , CM000681.2:g.18060044T>C	GRCh38
NC_000019.9:g.18170854T>C , CM000681.1:g.18170854T>C	GRCh37
NC_000019.8:g.18031854T>C	NCBI36
NG_007366.2:g.43906A>G , LRG_72:g.43906A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1833A>G MANE Select	ENSP00000472165.2:p.Ala611=
ENST00000593993.6:c.1833A>G	ENSP00000472165.2:p.Ala611=
ENST00000600835.6:c.1833A>G	ENSP00000470788.1:p.Ala611=
NM_001290023.1:c.1833A>G	NP_001276952.1:p.Ala611=
NM_001290024.1:c.1953A>G	NP_001276953.1:p.Ala651=
NM_005535.2:c.1833A>G	NP_005526.1:p.Ala611=
XM_006722741.2:c.1953A>G	XP_006722804.2:p.Ala651=
XM_011527966.1:c.1986A>G	XP_011526268.1:p.Ala662=
XM_011527967.1:c.1974A>G	XP_011526269.1:p.Ala658=
XM_011527968.1:c.1965A>G	XP_011526270.1:p.Ala655=
XM_011527969.1:c.1953A>G	XP_011526271.1:p.Ala651=
XM_011527970.1:c.1986A>G	XP_011526272.1:p.Ala662=
XM_011527971.1:c.1986A>G	XP_011526273.1:p.Ala662=
XM_011527972.1:c.1986A>G	XP_011526274.1:p.Ala662=
XM_011527973.1:c.1866A>G	XP_011526275.1:p.Ala622=
XM_011527974.1:c.1854A>G	XP_011526276.1:p.Ala618=
XM_011527975.1:c.1953A>G	XP_011526277.1:p.Ala651=
XM_006722741.3:c.1953A>G	XP_006722804.2:p.Ala651=
XM_011527966.2:c.1986A>G	XP_011526268.1:p.Ala662=
XM_011527967.2:c.1974A>G	XP_011526269.1:p.Ala658=
XM_011527968.3:c.1965A>G	XP_011526270.1:p.Ala655=
XM_011527969.2:c.1953A>G	XP_011526271.1:p.Ala651=
XM_011527970.2:c.1986A>G	XP_011526272.1:p.Ala662=
XM_011527971.3:c.1986A>G	XP_011526273.1:p.Ala662=
XM_011527972.3:c.1986A>G	XP_011526274.1:p.Ala662=
XM_011527973.2:c.1866A>G	XP_011526275.1:p.Ala622=
XM_011527974.2:c.1854A>G	XP_011526276.1:p.Ala618=
XM_011527975.2:c.1953A>G	XP_011526277.1:p.Ala651=
XM_017026762.1:c.1251A>G	XP_016882251.1:p.Ala417=
NM_001290023.2:c.1833A>G	NP_001276952.1:p.Ala611=
NM_005535.3:c.1833A>G MANE Select	NP_005526.1:p.Ala611=