Canonical Allele Identifier: CA1595017193
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320180G= , CM000667.2:g.159320180G= GRCh38
NC_000005.9:g.158747188G= , CM000667.1:g.158747188G= GRCh37
NC_000005.8:g.158679766G= NCBI36
NG_009618.1:g.15294C= , LRG_71:g.15294C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+126C= ENSP00000512849.1:n.67+126C=
ENST00000696751.1:c.*192+126C= ENSP00000512850.1:n.*192+126C=
ENST00000231228.3:c.697+126C= MANE Select ENSP00000231228.2:n.697+126C=
ENST00000231228.2:c.697+126C= ENSP00000231228.2:n.697+126C=
NM_002187.2:c.697+126C= , LRG_71t1:c.697+126C= NP_002178.2:n.697+126C=
NM_002187.3:c.697+126C= MANE Select NP_002178.2:n.697+126C=
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