Canonical Allele Identifier: CA806427385

Gene: IL12B

Linked Data

• dbSNP Id: rs1453027163
• gnomAD v3: 5-159315066-TC-T
• gnomAD v4: 5-159315066-TC-T
• MyVariant Identifiers: chr5:g.158742075del (hg19) ; chr5:g.159315067del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315068del , CM000667.2:g.159315068del	GRCh38
NC_000005.9:g.158742076del , CM000667.1:g.158742076del	GRCh37
NC_000005.8:g.158674654del	NCBI36
NG_009618.1:g.20407del , LRG_71:g.20407del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1034del	ENSP00000512849.1:n.*1034del
ENST00000696751.1:c.*1516del	ENSP00000512850.1:n.*1516del
ENST00000231228.3:c.*1034del MANE Select	ENSP00000231228.2:n.*1034del
ENST00000231228.2:c.*1034del	ENSP00000231228.2:n.*1034del
NM_002187.2:c.*1034del , LRG_71t1:c.*1034del	NP_002178.2:n.*1034del
XR_941138.1:n.364-150del
XR_941138.2:n.431-150del
NM_002187.3:c.*1034del MANE Select	NP_002178.2:n.*1034del