Canonical Allele Identifier: CA1595017233

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320258_159320259delinsCA , CM000667.2:g.159320258_159320259delinsCA	GRCh38
NC_000005.9:g.158747266_158747267delinsCA , CM000667.1:g.158747266_158747267delinsCA	GRCh37
NC_000005.8:g.158679844_158679845delinsCA	NCBI36
NG_009618.1:g.15215_15216delinsTG , LRG_71:g.15215_15216delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+47_67+48delinsTG	ENSP00000512849.1:n.67+47_67+48delinsTG
ENST00000696751.1:c.*192+47_*192+48delinsTG	ENSP00000512850.1:n.*192+47_*192+48delinsTG
ENST00000231228.3:c.697+47_697+48delinsTG MANE Select	ENSP00000231228.2:n.697+47_697+48delinsTG
ENST00000231228.2:c.697+47_697+48delinsTG	ENSP00000231228.2:n.697+47_697+48delinsTG
NM_002187.2:c.697+47_697+48delinsTG , LRG_71t1:c.697+47_697+48delinsTG	NP_002178.2:n.697+47_697+48delinsTG
NM_002187.3:c.697+47_697+48delinsTG MANE Select	NP_002178.2:n.697+47_697+48delinsTG