Canonical Allele Identifier: CA1139995595

Gene: IL12RB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67370377G= , CM000663.2:g.67370377G=	GRCh38
NC_000001.10:g.67836060G= , CM000663.1:g.67836060G=	GRCh37
NC_000001.9:g.67608648G=	NCBI36
NG_032977.1:g.68014G=
NG_032977.2:g.68027G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696754.1:c.1460-2059G=	ENSP00000512852.1:n.1460-2059G=
ENST00000696755.1:c.1460-2059G=	ENSP00000512853.1:n.1460-2059G=
ENST00000696757.1:c.1460-2059G=	ENSP00000512854.1:n.1460-2059G=
ENST00000696758.1:c.*648-2059G=	ENSP00000512855.1:n.*648-2059G=
ENST00000696759.1:c.1460-2059G=	ENSP00000512856.1:n.1460-2059G=
ENST00000696762.1:n.1486-2059G=
ENST00000696763.1:n.552-2059G=
ENST00000541374.6:c.1459+2352G=	ENSP00000445276.3:n.1459+2352G=
ENST00000648487.1:c.1460-2059G=	ENSP00000497959.1:n.1460-2059G=
ENST00000674203.2:c.1460-2059G= MANE Select	ENSP00000501329.1:n.1460-2059G=
ENST00000262345.5:c.1460-2059G=	ENSP00000262345.1:n.1460-2059G=
ENST00000371000.5:c.1460-2059G=	ENSP00000360039.1:n.1460-2059G=
ENST00000541374.5:c.1460-2059G=	ENSP00000445276.2:n.1460-2059G=
ENST00000544434.5:c.1459+2352G=	ENSP00000442443.1:n.1459+2352G=
NM_001258214.1:c.1460-2059G=	NP_001245143.1:n.1460-2059G=
NM_001258215.1:c.1459+2352G=	NP_001245144.1:n.1459+2352G=
NM_001258216.1:c.1460-2059G=	NP_001245145.1:n.1460-2059G=
NM_001559.2:c.1460-2059G=	NP_001550.1:n.1460-2059G=
NR_047583.1:n.2100-2059G=
NR_047584.1:n.2100-2059G=
XM_005270825.1:c.1460-2059G=	XP_005270882.1:n.1460-2059G=
XM_005270827.1:c.1460-2059G=	XP_005270884.1:n.1460-2059G=
XM_005270828.2:c.1460-2059G=	XP_005270885.1:n.1460-2059G=
XM_006710617.1:c.1459+2352G=	XP_006710680.1:n.1459+2352G=
XM_011541383.1:c.1460-2059G=	XP_011539685.1:n.1460-2059G=
XM_011541384.1:c.1460-2059G=	XP_011539686.1:n.1460-2059G=
XM_011541385.1:c.1460-2059G=	XP_011539687.1:n.1460-2059G=
NM_001319233.1:c.1460-2059G=	NP_001306162.1:n.1460-2059G=
XM_005270825.2:c.1460-2059G=	XP_005270882.1:n.1460-2059G=
XM_005270827.2:c.1460-2059G=	XP_005270884.1:n.1460-2059G=
XM_005270828.3:c.1460-2059G=	XP_005270885.1:n.1460-2059G=
XM_006710617.2:c.1459+2352G=	XP_006710680.1:n.1459+2352G=
XM_011541383.2:c.1460-2059G=	XP_011539685.1:n.1460-2059G=
XM_011541384.2:c.1460-2059G=	XP_011539686.1:n.1460-2059G=
XM_017001203.1:c.1460-2059G=	XP_016856692.1:n.1460-2059G=
XM_017001204.1:c.1460-1804G=	XP_016856693.1:n.1460-1804G=
NM_001374259.2:c.1460-2059G= MANE Select	NP_001361188.1:n.1460-2059G=
NM_001559.3:c.1460-2059G=	NP_001550.1:n.1460-2059G=