Canonical Allele Identifier: CA1595018016

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321988_159321989delinsCA , CM000667.2:g.159321988_159321989delinsCA	GRCh38
NC_000005.9:g.158748996_158748997delinsCA , CM000667.1:g.158748996_158748997delinsCA	GRCh37
NC_000005.8:g.158681574_158681575delinsCA	NCBI36
NG_009618.1:g.13485_13486delinsTG , LRG_71:g.13485_13486delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-1469_-148-1468delinsTG	ENSP00000512849.1:n.-148-1469_-148-1468de...
ENST00000696751.1:c.364+1065_364+1066delinsTG	ENSP00000512850.1:n.364+1065_364+1066deli...
ENST00000231228.3:c.482+405_482+406delinsTG MANE Select	ENSP00000231228.2:n.482+405_482+406delins...
ENST00000231228.2:c.482+405_482+406delinsTG	ENSP00000231228.2:n.482+405_482+406delins...
NM_002187.2:c.482+405_482+406delinsTG , LRG_71t1:c.482+405_482+406delinsTG	NP_002178.2:n.482+405_482+406delinsTG
XR_001742945.1:n.147+1392_147+1393delinsCA
NM_002187.3:c.482+405_482+406delinsTG MANE Select	NP_002178.2:n.482+405_482+406delinsTG