Canonical Allele Identifier: CA1595020830

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328810_159328811delinsAG , CM000667.2:g.159328810_159328811delinsAG	GRCh38
NC_000005.9:g.158755818_158755819delinsAG , CM000667.1:g.158755818_158755819delinsAG	GRCh37
NC_000005.8:g.158688396_158688397delinsAG	NCBI36
NG_009618.1:g.6663_6664delinsCT , LRG_71:g.6663_6664delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+1621_-149+1622delinsCT	ENSP00000512849.1:n.-149+1621_-149+1622delinsCT
ENST00000696751.1:c.-1+1621_-1+1622delinsCT	ENSP00000512850.1:n.-1+1621_-1+1622delinsCT
ENST00000696752.1:n.432+1621_432+1622delinsCT
ENST00000231228.3:c.-1+1621_-1+1622delinsCT MANE Select	ENSP00000231228.2:n.-1+1621_-1+1622delinsCT
ENST00000231228.2:c.-1+1621_-1+1622delinsCT	ENSP00000231228.2:n.-1+1621_-1+1622delinsCT
NM_002187.2:c.-1+1621_-1+1622delinsCT , LRG_71t1:c.-1+1621_-1+1622delinsCT	NP_002178.2:n.-1+1621_-1+1622delinsCT
NM_002187.3:c.-1+1621_-1+1622delinsCT MANE Select	NP_002178.2:n.-1+1621_-1+1622delinsCT