Canonical Allele Identifier: CA2514874859

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327451_159327452insGACAACTGCTTCTTCGCAGCAA , CM000667.2:g.159327451_159327452insGACAACTGCTTCTTCGCAGCAA	GRCh38
NC_000005.9:g.158754459_158754460insGACAACTGCTTCTTCGCAGCAA , CM000667.1:g.158754459_158754460insGACAACTGCTTCTTCGCAGCAA	GRCh37
NC_000005.8:g.158687037_158687038insGACAACTGCTTCTTCGCAGCAA	NCBI36
NG_009618.1:g.8022_8023insTTGCTGCGAAGAAGCAGTTGTC , LRG_71:g.8022_8023insTTGCTGCGAAGAAGCAGTTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+2980_-149+2981insTTGCTGCGAAGAAGCAGTTGTC	ENSP00000512849.1:n.-149+2980_-149+2981insTTGCTGCGAAGAAGCAGTT...
ENST00000696751.1:c.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC	ENSP00000512850.1:n.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC
ENST00000696752.1:n.433-670_433-669insTTGCTGCGAAGAAGCAGTTGTC
ENST00000231228.3:c.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC MANE Select	ENSP00000231228.2:n.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC
ENST00000231228.2:c.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC	ENSP00000231228.2:n.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC
NM_002187.2:c.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC , LRG_71t1:c.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC	NP_002178.2:n.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC
NM_002187.3:c.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC MANE Select	NP_002178.2:n.1-670_1-669insTTGCTGCGAAGAAGCAGTTGTC