Canonical Allele Identifier: CA1595017239
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320272C= , CM000667.2:g.159320272C= GRCh38
NC_000005.9:g.158747280C= , CM000667.1:g.158747280C= GRCh37
NC_000005.8:g.158679858C= NCBI36
NG_009618.1:g.15202G= , LRG_71:g.15202G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+34G= ENSP00000512849.1:n.67+34G=
ENST00000696751.1:c.*192+34G= ENSP00000512850.1:n.*192+34G=
ENST00000231228.3:c.697+34G= MANE Select ENSP00000231228.2:n.697+34G=
ENST00000231228.2:c.697+34G= ENSP00000231228.2:n.697+34G=
NM_002187.2:c.697+34G= , LRG_71t1:c.697+34G= NP_002178.2:n.697+34G=
NM_002187.3:c.697+34G= MANE Select NP_002178.2:n.697+34G=