Canonical Allele Identifier: CA2326165149

Gene: IL12RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18059932_18059934delinsCTG , CM000681.2:g.18059932_18059934delinsCTG	GRCh38
NC_000019.9:g.18170742_18170744delinsCTG , CM000681.1:g.18170742_18170744delinsCTG	GRCh37
NC_000019.8:g.18031742_18031744delinsCTG	NCBI36
NG_007366.2:g.44016_44018delinsCAG , LRG_72:g.44016_44018delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593993.7:c.1943_1945delinsCAG MANE Select	ENSP00000472165.2:p.Thr648=
ENST00000593993.6:c.1943_1945delinsCAG	ENSP00000472165.2:p.Thr648=
ENST00000600835.6:c.1943_1945delinsCAG	ENSP00000470788.1:p.Thr648=
NM_001290023.1:c.1943_1945delinsCAG	NP_001276952.1:p.Thr648=
NM_001290024.1:c.2063_2065delinsCAG	NP_001276953.1:p.Thr688=
NM_005535.2:c.1943_1945delinsCAG	NP_005526.1:p.Thr648=
XM_006722741.2:c.2063_2065delinsCAG	XP_006722804.2:p.Thr688=
XM_011527966.1:c.2096_2098delinsCAG	XP_011526268.1:p.Thr699=
XM_011527967.1:c.2084_2086delinsCAG	XP_011526269.1:p.Thr695=
XM_011527968.1:c.2075_2077delinsCAG	XP_011526270.1:p.Thr692=
XM_011527969.1:c.2063_2065delinsCAG	XP_011526271.1:p.Thr688=
XM_011527970.1:c.2096_2098delinsCAG	XP_011526272.1:p.Thr699=
XM_011527971.1:c.2096_2098delinsCAG	XP_011526273.1:p.Thr699=
XM_011527972.1:c.2096_2098delinsCAG	XP_011526274.1:p.Thr699=
XM_011527973.1:c.1976_1978delinsCAG	XP_011526275.1:p.Thr659=
XM_011527974.1:c.1964_1966delinsCAG	XP_011526276.1:p.Thr655=
XM_011527975.1:c.2063_2065delinsCAG	XP_011526277.1:p.Thr688=
XM_006722741.3:c.2063_2065delinsCAG	XP_006722804.2:p.Thr688=
XM_011527966.2:c.2096_2098delinsCAG	XP_011526268.1:p.Thr699=
XM_011527967.2:c.2084_2086delinsCAG	XP_011526269.1:p.Thr695=
XM_011527968.3:c.2075_2077delinsCAG	XP_011526270.1:p.Thr692=
XM_011527969.2:c.2063_2065delinsCAG	XP_011526271.1:p.Thr688=
XM_011527970.2:c.2096_2098delinsCAG	XP_011526272.1:p.Thr699=
XM_011527971.3:c.2096_2098delinsCAG	XP_011526273.1:p.Thr699=
XM_011527972.3:c.2096_2098delinsCAG	XP_011526274.1:p.Thr699=
XM_011527973.2:c.1976_1978delinsCAG	XP_011526275.1:p.Thr659=
XM_011527974.2:c.1964_1966delinsCAG	XP_011526276.1:p.Thr655=
XM_011527975.2:c.2063_2065delinsCAG	XP_011526277.1:p.Thr688=
XM_017026762.1:c.1361_1363delinsCAG	XP_016882251.1:p.Thr454=
NM_001290023.2:c.1943_1945delinsCAG	NP_001276952.1:p.Thr648=
NM_005535.3:c.1943_1945delinsCAG MANE Select	NP_005526.1:p.Thr648=