Canonical Allele Identifier: CA1595017133

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320067_159320068delinsTG , CM000667.2:g.159320067_159320068delinsTG	GRCh38
NC_000005.9:g.158747075_158747076delinsTG , CM000667.1:g.158747075_158747076delinsTG	GRCh37
NC_000005.8:g.158679653_158679654delinsTG	NCBI36
NG_009618.1:g.15406_15407delinsCA , LRG_71:g.15406_15407delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+238_67+239delinsCA	ENSP00000512849.1:n.67+238_67+239delinsCA
ENST00000696751.1:c.*192+238_*192+239delinsCA	ENSP00000512850.1:n.*192+238_*192+239delinsCA
ENST00000231228.3:c.697+238_697+239delinsCA MANE Select	ENSP00000231228.2:n.697+238_697+239delinsCA
ENST00000231228.2:c.697+238_697+239delinsCA	ENSP00000231228.2:n.697+238_697+239delinsCA
NM_002187.2:c.697+238_697+239delinsCA , LRG_71t1:c.697+238_697+239delinsCA	NP_002178.2:n.697+238_697+239delinsCA
NM_002187.3:c.697+238_697+239delinsCA MANE Select	NP_002178.2:n.697+238_697+239delinsCA