Canonical Allele Identifier: CA2522860883

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327455_159327456insCTTCGCCGCAACCGGTATCACCGACGGCAA , CM000667.2:g.159327455_159327456insCTTCGCCGCAACCGGTATCACCGACGGCAA	GRCh38
NC_000005.9:g.158754463_158754464insCTTCGCCGCAACCGGTATCACCGACGGCAA , CM000667.1:g.158754463_158754464insCTTCGCCGCAACCGGTATCACCGACGGCAA	GRCh37
NC_000005.8:g.158687041_158687042insCTTCGCCGCAACCGGTATCACCGACGGCAA	NCBI36
NG_009618.1:g.8018_8019insTTGCCGTCGGTGATACCGGTTGCGGCGAAG , LRG_71:g.8018_8019insTTGCCGTCGGTGATACCGGTTGCGGCGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+2976_-149+2977insTTGCCGTCGGTGATACCGGTTGCGGCGAAG	ENSP00000512849.1:n.-149+2976_-149+2977insTTGCCGTCGGTGATACCGG...
ENST00000696751.1:c.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG	ENSP00000512850.1:n.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCG...
ENST00000696752.1:n.433-674_433-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG
ENST00000231228.3:c.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG MANE Select	ENSP00000231228.2:n.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCG...
ENST00000231228.2:c.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG	ENSP00000231228.2:n.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCG...
NM_002187.2:c.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG , LRG_71t1:c.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG	NP_002178.2:n.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG
NM_002187.3:c.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG MANE Select	NP_002178.2:n.1-674_1-673insTTGCCGTCGGTGATACCGGTTGCGGCGAAG