Canonical Allele Identifier: CA16056291

Gene: IL12RB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67315434A>G , CM000663.2:g.67315434A>G	GRCh38
NC_000001.10:g.67781117A>G , CM000663.1:g.67781117A>G	GRCh37
NC_000001.9:g.67553705A>G	NCBI36
NG_032977.1:g.13071A>G
NG_032977.2:g.13084A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696754.1:c.-37+1434A>G	ENSP00000512852.1:n.-37+1434A>G
ENST00000696755.1:c.-36-4899A>G	ENSP00000512853.1:n.-36-4899A>G
ENST00000696756.1:n.124-4899A>G
ENST00000696757.1:c.-36-4899A>G	ENSP00000512854.1:n.-36-4899A>G
ENST00000696758.1:c.-32-4903A>G	ENSP00000512855.1:n.-32-4903A>G
ENST00000696759.1:c.-37+1434A>G	ENSP00000512856.1:n.-37+1434A>G
ENST00000696760.1:n.167+1434A>G
ENST00000696761.1:c.-33+1434A>G	ENSP00000512857.1:n.-33+1434A>G
ENST00000541374.6:c.-37+1434A>G	ENSP00000445276.3:n.-37+1434A>G
ENST00000648487.1:c.-33+1434A>G	ENSP00000497959.1:n.-33+1434A>G
ENST00000674203.2:c.-37+1434A>G MANE Select	ENSP00000501329.1:n.-37+1434A>G
ENST00000262345.5:c.-36-4899A>G	ENSP00000262345.1:n.-36-4899A>G
ENST00000371000.5:c.-37+1434A>G	ENSP00000360039.1:n.-37+1434A>G
ENST00000541374.5:c.-36-4899A>G	ENSP00000445276.2:n.-36-4899A>G
ENST00000544434.5:c.-36-4899A>G	ENSP00000442443.1:n.-36-4899A>G
NM_001258214.1:c.-37+1434A>G	NP_001245143.1:n.-37+1434A>G
NM_001258215.1:c.-36-4899A>G	NP_001245144.1:n.-36-4899A>G
NM_001258216.1:c.-36-4899A>G	NP_001245145.1:n.-36-4899A>G
NM_001559.2:c.-36-4899A>G	NP_001550.1:n.-36-4899A>G
NR_047583.1:n.605-4899A>G
NR_047584.1:n.605-4899A>G
XM_005270825.1:c.-37+1434A>G	XP_005270882.1:n.-37+1434A>G
XM_005270827.1:c.-33+1434A>G	XP_005270884.1:n.-33+1434A>G
XM_005270828.2:c.-32-4903A>G	XP_005270885.1:n.-32-4903A>G
XM_006710617.1:c.-37+1434A>G	XP_006710680.1:n.-37+1434A>G
XM_011541383.1:c.-37+1434A>G	XP_011539685.1:n.-37+1434A>G
XM_011541384.1:c.-37+1434A>G	XP_011539686.1:n.-37+1434A>G
XM_011541385.1:c.-33+1434A>G	XP_011539687.1:n.-33+1434A>G
NM_001319233.1:c.-33+1434A>G	NP_001306162.1:n.-33+1434A>G
XM_005270825.2:c.-37+1434A>G	XP_005270882.1:n.-37+1434A>G
XM_005270827.2:c.-33+1434A>G	XP_005270884.1:n.-33+1434A>G
XM_005270828.3:c.-32-4903A>G	XP_005270885.1:n.-32-4903A>G
XM_006710617.2:c.-37+1434A>G	XP_006710680.1:n.-37+1434A>G
XM_011541383.2:c.-37+1434A>G	XP_011539685.1:n.-37+1434A>G
XM_011541384.2:c.-37+1434A>G	XP_011539686.1:n.-37+1434A>G
XM_017001203.1:c.-36-4899A>G	XP_016856692.1:n.-36-4899A>G
XM_017001204.1:c.-37+1434A>G	XP_016856693.1:n.-37+1434A>G
NM_001374259.2:c.-37+1434A>G MANE Select	NP_001361188.1:n.-37+1434A>G
NM_001559.3:c.-36-4899A>G	NP_001550.1:n.-36-4899A>G