Canonical Allele Identifier: CA1139921611

Gene: IL12RB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67395837C= , CM000663.2:g.67395837C=	GRCh38
NC_000001.10:g.67861520C= , CM000663.1:g.67861520C=	GRCh37
NC_000001.9:g.67634108C=	NCBI36
NG_032977.1:g.93474C=
NG_032977.2:g.93487C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374259.2:c.2337C= MANE Select	NP_001361188.1:p.Pro779=
ENST00000674203.2:c.2337C= MANE Select	ENSP00000501329.1:p.Pro779=
NM_001258214.1:c.*257C=	NP_001245143.1:n.*257C=
NM_001258215.1:c.2079C=	NP_001245144.1:p.Pro693=
NM_001258216.1:c.*238C=	NP_001245145.1:n.*238C=
NM_001319233.1:c.*257C=	NP_001306162.1:n.*257C=
NM_001559.2:c.2337C=	NP_001550.1:p.Pro779=
NM_001559.3:c.2337C=	NP_001550.1:p.Pro779=
NR_047583.1:n.2727C=
NR_047584.1:n.3070C=
ENST00000262345.5:c.2337C=	ENSP00000262345.1:p.Pro779=
ENST00000541374.5:c.*238C=	ENSP00000445276.2:n.*238C=
ENST00000541374.6:c.*238C=	ENSP00000445276.3:n.*238C=
ENST00000544434.5:c.2079C=	ENSP00000442443.1:p.Pro693=
ENST00000648487.1:c.2337C=	ENSP00000497959.1:p.Pro779=
ENST00000696754.1:c.*238C=	ENSP00000512852.1:n.*238C=
ENST00000696755.1:c.*238C=	ENSP00000512853.1:n.*238C=
ENST00000696757.1:c.*257C=	ENSP00000512854.1:n.*257C=
ENST00000696758.1:c.*1434C=	ENSP00000512855.1:n.*1434C=
ENST00000696759.1:c.*374C=	ENSP00000512856.1:n.*374C=
ENST00000696763.1:n.1329C=
XM_005270825.1:c.2337C=	XP_005270882.1:p.Pro779=
XM_005270825.2:c.2337C=	XP_005270882.1:p.Pro779=
XM_005270827.1:c.2337C=	XP_005270884.1:p.Pro779=
XM_005270827.2:c.2337C=	XP_005270884.1:p.Pro779=
XM_005270828.2:c.2337C=	XP_005270885.1:p.Pro779=
XM_005270828.3:c.2337C=	XP_005270885.1:p.Pro779=
XM_006710617.1:c.2079C=	XP_006710680.1:p.Pro693=
XM_006710617.2:c.2079C=	XP_006710680.1:p.Pro693=
XM_011541383.1:c.2337C=	XP_011539685.1:p.Pro779=
XM_011541383.2:c.2337C=	XP_011539685.1:p.Pro779=
XM_011541384.1:c.2178C=	XP_011539686.1:p.Pro726=
XM_011541384.2:c.2178C=	XP_011539686.1:p.Pro726=
XM_011541385.1:c.*257C=	XP_011539687.1:n.*257C=
XM_017001203.1:c.*257C=	XP_016856692.1:n.*257C=