Canonical Allele Identifier: CA806428088
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1173420613

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316158T>C , CM000667.2:g.159316158T>C GRCh38
NC_000005.9:g.158743166T>C , CM000667.1:g.158743166T>C GRCh37
NC_000005.8:g.158675744T>C NCBI36
NG_009618.1:g.19316A>G , LRG_71:g.19316A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1-58A>G ENSP00000512849.1:n.*1-58A>G
ENST00000696751.1:c.*483-58A>G ENSP00000512850.1:n.*483-58A>G
ENST00000231228.3:c.*1-58A>G MANE Select ENSP00000231228.2:n.*1-58A>G
ENST00000231228.2:c.*1-58A>G ENSP00000231228.2:n.*1-58A>G
NM_002187.2:c.*1-58A>G , LRG_71t1:c.*1-58A>G NP_002178.2:n.*1-58A>G
NM_002187.3:c.*1-58A>G MANE Select NP_002178.2:n.*1-58A>G