Canonical Allele Identifier: CA1595017246
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320281G= , CM000667.2:g.159320281G= GRCh38
NC_000005.9:g.158747289G= , CM000667.1:g.158747289G= GRCh37
NC_000005.8:g.158679867G= NCBI36
NG_009618.1:g.15193C= , LRG_71:g.15193C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+25C= ENSP00000512849.1:n.67+25C=
ENST00000696751.1:c.*192+25C= ENSP00000512850.1:n.*192+25C=
ENST00000231228.3:c.697+25C= MANE Select ENSP00000231228.2:n.697+25C=
ENST00000231228.2:c.697+25C= ENSP00000231228.2:n.697+25C=
NM_002187.2:c.697+25C= , LRG_71t1:c.697+25C= NP_002178.2:n.697+25C=
NM_002187.3:c.697+25C= MANE Select NP_002178.2:n.697+25C=