Canonical Allele Identifier: CA1595017112

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320021_159320022delinsCA , CM000667.2:g.159320021_159320022delinsCA	GRCh38
NC_000005.9:g.158747029_158747030delinsCA , CM000667.1:g.158747029_158747030delinsCA	GRCh37
NC_000005.8:g.158679607_158679608delinsCA	NCBI36
NG_009618.1:g.15452_15453delinsTG , LRG_71:g.15452_15453delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+284_67+285delinsTG	ENSP00000512849.1:n.67+284_67+285delinsTG
ENST00000696751.1:c.*192+284_*192+285delinsTG	ENSP00000512850.1:n.*192+284_*192+285delinsTG
ENST00000231228.3:c.697+284_697+285delinsTG MANE Select	ENSP00000231228.2:n.697+284_697+285delinsTG
ENST00000231228.2:c.697+284_697+285delinsTG	ENSP00000231228.2:n.697+284_697+285delinsTG
NM_002187.2:c.697+284_697+285delinsTG , LRG_71t1:c.697+284_697+285delinsTG	NP_002178.2:n.697+284_697+285delinsTG
NM_002187.3:c.697+284_697+285delinsTG MANE Select	NP_002178.2:n.697+284_697+285delinsTG