Canonical Allele Identifier: CA1595020241

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327395_159327400delinsCAGGAA , CM000667.2:g.159327395_159327400delinsCAGGAA	GRCh38
NC_000005.9:g.158754403_158754408delinsCAGGAA , CM000667.1:g.158754403_158754408delinsCAGGAA	GRCh37
NC_000005.8:g.158686981_158686986delinsCAGGAA	NCBI36
NG_009618.1:g.8074_8079delinsTTCCTG , LRG_71:g.8074_8079delinsTTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3032_-149+3037delinsTTCCTG	ENSP00000512849.1:n.-149+3032_-149+3037delinsTTCCTG
ENST00000696751.1:c.1-618_1-613delinsTTCCTG	ENSP00000512850.1:n.1-618_1-613delinsTTCCTG
ENST00000696752.1:n.433-618_433-613delinsTTCCTG
ENST00000231228.3:c.1-618_1-613delinsTTCCTG MANE Select	ENSP00000231228.2:n.1-618_1-613delinsTTCCTG
ENST00000231228.2:c.1-618_1-613delinsTTCCTG	ENSP00000231228.2:n.1-618_1-613delinsTTCCTG
NM_002187.2:c.1-618_1-613delinsTTCCTG , LRG_71t1:c.1-618_1-613delinsTTCCTG	NP_002178.2:n.1-618_1-613delinsTTCCTG
NM_002187.3:c.1-618_1-613delinsTTCCTG MANE Select	NP_002178.2:n.1-618_1-613delinsTTCCTG