Canonical Allele Identifier: CA129827798
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs975481253

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159321989_159321991del , CM000667.2:g.159321989_159321991del GRCh38
NC_000005.9:g.158748997_158748999del , CM000667.1:g.158748997_158748999del GRCh37
NC_000005.8:g.158681575_158681577del NCBI36
NG_009618.1:g.13483_13485del , LRG_71:g.13483_13485del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1471_-148-1469del ENSP00000512849.1:n.-148-1471_-148-1469de...
ENST00000696751.1:c.364+1063_364+1065del ENSP00000512850.1:n.364+1063_364+1065del
ENST00000231228.3:c.482+403_482+405del MANE Select ENSP00000231228.2:n.482+403_482+405del
ENST00000231228.2:c.482+403_482+405del ENSP00000231228.2:n.482+403_482+405del
NM_002187.2:c.482+403_482+405del , LRG_71t1:c.482+403_482+405del NP_002178.2:n.482+403_482+405del
XR_001742945.1:n.147+1393_147+1395del
NM_002187.3:c.482+403_482+405del MANE Select NP_002178.2:n.482+403_482+405del