Canonical Allele Identifier: CA1595020753

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328621_159328623delinsGCA , CM000667.2:g.159328621_159328623delinsGCA	GRCh38
NC_000005.9:g.158755629_158755631delinsGCA , CM000667.1:g.158755629_158755631delinsGCA	GRCh37
NC_000005.8:g.158688207_158688209delinsGCA	NCBI36
NG_009618.1:g.6851_6853delinsTGC , LRG_71:g.6851_6853delinsTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+1809_-149+1811delinsTGC	ENSP00000512849.1:n.-149+1809_-149+1811de...
ENST00000696751.1:c.-1+1809_-1+1811delinsTGC	ENSP00000512850.1:n.-1+1809_-1+1811delins...
ENST00000696752.1:n.432+1809_432+1811delinsTGC
ENST00000231228.3:c.-1+1809_-1+1811delinsTGC MANE Select	ENSP00000231228.2:n.-1+1809_-1+1811delins...
ENST00000231228.2:c.-1+1809_-1+1811delinsTGC	ENSP00000231228.2:n.-1+1809_-1+1811delins...
NM_002187.2:c.-1+1809_-1+1811delinsTGC , LRG_71t1:c.-1+1809_-1+1811delinsTGC	NP_002178.2:n.-1+1809_-1+1811delinsTGC
NM_002187.3:c.-1+1809_-1+1811delinsTGC MANE Select	NP_002178.2:n.-1+1809_-1+1811delinsTGC