Canonical Allele Identifier: CA1083506159
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1753983526

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316008del , CM000667.2:g.159316008del GRCh38
NC_000005.9:g.158743016del , CM000667.1:g.158743016del GRCh37
NC_000005.8:g.158675594del NCBI36
NG_009618.1:g.19466del , LRG_71:g.19466del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*93del ENSP00000512849.1:n.*93del
ENST00000696751.1:c.*575del ENSP00000512850.1:n.*575del
ENST00000231228.3:c.*93del MANE Select ENSP00000231228.2:n.*93del
ENST00000231228.2:c.*93del ENSP00000231228.2:n.*93del
NM_002187.2:c.*93del , LRG_71t1:c.*93del NP_002178.2:n.*93del
NM_002187.3:c.*93del MANE Select NP_002178.2:n.*93del