Canonical Allele Identifier: CA2676264571

Gene: IL12B

Linked Data

• gnomAD v4: 5-159315986-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315987del , CM000667.2:g.159315987del	GRCh38
NC_000005.9:g.158742995del , CM000667.1:g.158742995del	GRCh37
NC_000005.8:g.158675573del	NCBI36
NG_009618.1:g.19487del , LRG_71:g.19487del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*114del	ENSP00000512849.1:n.*114del
ENST00000696751.1:c.*596del	ENSP00000512850.1:n.*596del
ENST00000231228.3:c.*114del MANE Select	ENSP00000231228.2:n.*114del
ENST00000231228.2:c.*114del	ENSP00000231228.2:n.*114del
NM_002187.2:c.*114del , LRG_71t1:c.*114del	NP_002178.2:n.*114del
NM_002187.3:c.*114del MANE Select	NP_002178.2:n.*114del