Canonical Allele Identifier: CA806428080
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1401180717

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316144A>G , CM000667.2:g.159316144A>G GRCh38
NC_000005.9:g.158743152A>G , CM000667.1:g.158743152A>G GRCh37
NC_000005.8:g.158675730A>G NCBI36
NG_009618.1:g.19330T>C , LRG_71:g.19330T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1-44T>C ENSP00000512849.1:n.*1-44T>C
ENST00000696751.1:c.*483-44T>C ENSP00000512850.1:n.*483-44T>C
ENST00000231228.3:c.*1-44T>C MANE Select ENSP00000231228.2:n.*1-44T>C
ENST00000231228.2:c.*1-44T>C ENSP00000231228.2:n.*1-44T>C
NM_002187.2:c.*1-44T>C , LRG_71t1:c.*1-44T>C NP_002178.2:n.*1-44T>C
NM_002187.3:c.*1-44T>C MANE Select NP_002178.2:n.*1-44T>C