Canonical Allele Identifier: CA2676264684
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316216_159316217insTGTAGATCT , CM000667.2:g.159316216_159316217insTGTAGATCT GRCh38
NC_000005.9:g.158743224_158743225insTGTAGATCT , CM000667.1:g.158743224_158743225insTGTAGATCT GRCh37
NC_000005.8:g.158675802_158675803insTGTAGATCT NCBI36
NG_009618.1:g.19257_19258insAGATCTACA , LRG_71:g.19257_19258insAGATCTACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*1-117_*1-116insAGATCTACA ENSP00000512849.1:n.*1-117_*1-116insAGATCTACA
ENST00000696751.1:c.*483-117_*483-116insAGATCTACA ENSP00000512850.1:n.*483-117_*483-116insAGATCTACA
ENST00000231228.3:c.*1-117_*1-116insAGATCTACA MANE Select ENSP00000231228.2:n.*1-117_*1-116insAGATCTACA
ENST00000231228.2:c.*1-117_*1-116insAGATCTACA ENSP00000231228.2:n.*1-117_*1-116insAGATCTACA
NM_002187.2:c.*1-117_*1-116insAGATCTACA , LRG_71t1:c.*1-117_*1-116insAGATCTACA NP_002178.2:n.*1-117_*1-116insAGATCTACA
NM_002187.3:c.*1-117_*1-116insAGATCTACA MANE Select NP_002178.2:n.*1-117_*1-116insAGATCTACA