Canonical Allele Identifier: CA806428028
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1384847293

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316140T>A , CM000667.2:g.159316140T>A GRCh38
NC_000005.9:g.158743148T>A , CM000667.1:g.158743148T>A GRCh37
NC_000005.8:g.158675726T>A NCBI36
NG_009618.1:g.19334A>T , LRG_71:g.19334A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1-40A>T ENSP00000512849.1:n.*1-40A>T
ENST00000696751.1:c.*483-40A>T ENSP00000512850.1:n.*483-40A>T
ENST00000231228.3:c.*1-40A>T MANE Select ENSP00000231228.2:n.*1-40A>T
ENST00000231228.2:c.*1-40A>T ENSP00000231228.2:n.*1-40A>T
NM_002187.2:c.*1-40A>T , LRG_71t1:c.*1-40A>T NP_002178.2:n.*1-40A>T
NM_002187.3:c.*1-40A>T MANE Select NP_002178.2:n.*1-40A>T