Canonical Allele Identifier: CA1595017099

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159319996_159319999delinsGGGA , CM000667.2:g.159319996_159319999delinsGGGA	GRCh38
NC_000005.9:g.158747004_158747007delinsGGGA , CM000667.1:g.158747004_158747007delinsGGGA	GRCh37
NC_000005.8:g.158679582_158679585delinsGGGA	NCBI36
NG_009618.1:g.15475_15478delinsTCCC , LRG_71:g.15475_15478delinsTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+307_67+310delinsTCCC	ENSP00000512849.1:n.67+307_67+310delinsTCCC
ENST00000696751.1:c.*192+307_*192+310delinsTCCC	ENSP00000512850.1:n.*192+307_*192+310delinsTCCC
ENST00000231228.3:c.697+307_697+310delinsTCCC MANE Select	ENSP00000231228.2:n.697+307_697+310delinsTCCC
ENST00000231228.2:c.697+307_697+310delinsTCCC	ENSP00000231228.2:n.697+307_697+310delinsTCCC
NM_002187.2:c.697+307_697+310delinsTCCC , LRG_71t1:c.697+307_697+310delinsTCCC	NP_002178.2:n.697+307_697+310delinsTCCC
NM_002187.3:c.697+307_697+310delinsTCCC MANE Select	NP_002178.2:n.697+307_697+310delinsTCCC