Canonical Allele Identifier: CA129827753
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs967354770

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159321924del , CM000667.2:g.159321924del GRCh38
NC_000005.9:g.158748932del , CM000667.1:g.158748932del GRCh37
NC_000005.8:g.158681510del NCBI36
NG_009618.1:g.13550del , LRG_71:g.13550del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1404del ENSP00000512849.1:n.-148-1404del
ENST00000696751.1:c.364+1130del ENSP00000512850.1:n.364+1130del
ENST00000231228.3:c.482+470del MANE Select ENSP00000231228.2:n.482+470del
ENST00000231228.2:c.482+470del ENSP00000231228.2:n.482+470del
NM_002187.2:c.482+470del , LRG_71t1:c.482+470del NP_002178.2:n.482+470del
XR_001742945.1:n.147+1328del
NM_002187.3:c.482+470del MANE Select NP_002178.2:n.482+470del