Canonical Allele Identifier: CA1595020787

Gene: IL12B

Linked Data

• dbSNP Id: rs1754230128

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328691_159328692insGGGTTGAAGAA , CM000667.2:g.159328691_159328692insGGGTTGAAGAA	GRCh38
NC_000005.9:g.158755699_158755700insGGGTTGAAGAA , CM000667.1:g.158755699_158755700insGGGTTGAAGAA	GRCh37
NC_000005.8:g.158688277_158688278insGGGTTGAAGAA	NCBI36
NG_009618.1:g.6782_6783insTTCTTCAACCC , LRG_71:g.6782_6783insTTCTTCAACCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+1740_-149+1741insTTCTTCAACCC	ENSP00000512849.1:n.-149+1740_-149+1741insTTCTTCAACCC
ENST00000696751.1:c.-1+1740_-1+1741insTTCTTCAACCC	ENSP00000512850.1:n.-1+1740_-1+1741insTTCTTCAACCC
ENST00000696752.1:n.432+1740_432+1741insTTCTTCAACCC
ENST00000231228.3:c.-1+1740_-1+1741insTTCTTCAACCC MANE Select	ENSP00000231228.2:n.-1+1740_-1+1741insTTCTTCAACCC
ENST00000231228.2:c.-1+1740_-1+1741insTTCTTCAACCC	ENSP00000231228.2:n.-1+1740_-1+1741insTTCTTCAACCC
NM_002187.2:c.-1+1740_-1+1741insTTCTTCAACCC , LRG_71t1:c.-1+1740_-1+1741insTTCTTCAACCC	NP_002178.2:n.-1+1740_-1+1741insTTCTTCAACCC
NM_002187.3:c.-1+1740_-1+1741insTTCTTCAACCC MANE Select	NP_002178.2:n.-1+1740_-1+1741insTTCTTCAACCC