Canonical Allele Identifier: CA1595017352

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320561_159320563delinsGGA , CM000667.2:g.159320561_159320563delinsGGA	GRCh38
NC_000005.9:g.158747569_158747571delinsGGA , CM000667.1:g.158747569_158747571delinsGGA	GRCh37
NC_000005.8:g.158680147_158680149delinsGGA	NCBI36
NG_009618.1:g.14911_14913delinsTCC , LRG_71:g.14911_14913delinsTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-43_-148-41delinsTCC	ENSP00000512849.1:n.-148-43_-148-41delins...
ENST00000696751.1:c.365-43_365-41delinsTCC	ENSP00000512850.1:n.365-43_365-41delinsTC...
ENST00000231228.3:c.483-43_483-41delinsTCC MANE Select	ENSP00000231228.2:n.483-43_483-41delinsTC...
ENST00000231228.2:c.483-43_483-41delinsTCC	ENSP00000231228.2:n.483-43_483-41delinsTC...
NM_002187.2:c.483-43_483-41delinsTCC , LRG_71t1:c.483-43_483-41delinsTCC	NP_002178.2:n.483-43_483-41delinsTCC
XR_001742945.1:n.112_114delinsGGA
NM_002187.3:c.483-43_483-41delinsTCC MANE Select	NP_002178.2:n.483-43_483-41delinsTCC