Canonical Allele Identifier: CA1595020056

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159326907_159326908delinsCT , CM000667.2:g.159326907_159326908delinsCT	GRCh38
NC_000005.9:g.158753915_158753916delinsCT , CM000667.1:g.158753915_158753916delinsCT	GRCh37
NC_000005.8:g.158686493_158686494delinsCT	NCBI36
NG_009618.1:g.8566_8567delinsAG , LRG_71:g.8566_8567delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3524_-149+3525delinsAG	ENSP00000512849.1:n.-149+3524_-149+3525delinsAG
ENST00000696751.1:c.1-126_1-125delinsAG	ENSP00000512850.1:n.1-126_1-125delinsAG
ENST00000696752.1:n.433-126_433-125delinsAG
ENST00000231228.3:c.1-126_1-125delinsAG MANE Select	ENSP00000231228.2:n.1-126_1-125delinsAG
ENST00000231228.2:c.1-126_1-125delinsAG	ENSP00000231228.2:n.1-126_1-125delinsAG
NM_002187.2:c.1-126_1-125delinsAG , LRG_71t1:c.1-126_1-125delinsAG	NP_002178.2:n.1-126_1-125delinsAG
NM_002187.3:c.1-126_1-125delinsAG MANE Select	NP_002178.2:n.1-126_1-125delinsAG