Canonical Allele Identifier: CA129832372
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs926138048

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328624_159328625del , CM000667.2:g.159328624_159328625del GRCh38
NC_000005.9:g.158755632_158755633del , CM000667.1:g.158755632_158755633del GRCh37
NC_000005.8:g.158688210_158688211del NCBI36
NG_009618.1:g.6851_6852del , LRG_71:g.6851_6852del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+1809_-149+1810del ENSP00000512849.1:n.-149+1809_-149+1810de...
ENST00000696751.1:c.-1+1809_-1+1810del ENSP00000512850.1:n.-1+1809_-1+1810del
ENST00000696752.1:n.432+1809_432+1810del
ENST00000231228.3:c.-1+1809_-1+1810del MANE Select ENSP00000231228.2:n.-1+1809_-1+1810del
ENST00000231228.2:c.-1+1809_-1+1810del ENSP00000231228.2:n.-1+1809_-1+1810del
NM_002187.2:c.-1+1809_-1+1810del , LRG_71t1:c.-1+1809_-1+1810del NP_002178.2:n.-1+1809_-1+1810del
NM_002187.3:c.-1+1809_-1+1810del MANE Select NP_002178.2:n.-1+1809_-1+1810del