Canonical Allele Identifier: CA2676264569

Gene: IL12B

Linked Data

• gnomAD v4: 5-159315979-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315986del , CM000667.2:g.159315986del	GRCh38
NC_000005.9:g.158742994del , CM000667.1:g.158742994del	GRCh37
NC_000005.8:g.158675572del	NCBI36
NG_009618.1:g.19494del , LRG_71:g.19494del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*121del	ENSP00000512849.1:n.*121del
ENST00000696751.1:c.*603del	ENSP00000512850.1:n.*603del
ENST00000231228.3:c.*121del MANE Select	ENSP00000231228.2:n.*121del
ENST00000231228.2:c.*121del	ENSP00000231228.2:n.*121del
NM_002187.2:c.*121del , LRG_71t1:c.*121del	NP_002178.2:n.*121del
NM_002187.3:c.*121del MANE Select	NP_002178.2:n.*121del