Canonical Allele Identifier: CA129826755
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs34446290

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320296dup , CM000667.2:g.159320296dup GRCh38
NC_000005.9:g.158747304dup , CM000667.1:g.158747304dup GRCh37
NC_000005.8:g.158679882dup NCBI36
NG_009618.1:g.15179dup , LRG_71:g.15179dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+11dup ENSP00000512849.1:n.67+11dup
ENST00000696751.1:c.*192+11dup ENSP00000512850.1:n.*192+11dup
ENST00000231228.3:c.697+11dup MANE Select ENSP00000231228.2:n.697+11dup
ENST00000231228.2:c.697+11dup ENSP00000231228.2:n.697+11dup
NM_002187.2:c.697+11dup , LRG_71t1:c.697+11dup NP_002178.2:n.697+11dup
NM_002187.3:c.697+11dup MANE Select NP_002178.2:n.697+11dup