Canonical Allele Identifier: CA1595017282
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320385C= , CM000667.2:g.159320385C= GRCh38
NC_000005.9:g.158747393C= , CM000667.1:g.158747393C= GRCh37
NC_000005.8:g.158679971C= NCBI36
NG_009618.1:g.15089G= , LRG_71:g.15089G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-13G= ENSP00000512849.1:n.-13G=
ENST00000696751.1:c.*113G= ENSP00000512850.1:n.*113G=
ENST00000231228.3:c.618G= MANE Select ENSP00000231228.2:p.Leu206=
ENST00000231228.2:c.618G= ENSP00000231228.2:p.Leu206=
NM_002187.2:c.618G= , LRG_71t1:c.618G= NP_002178.2:p.Leu206=
NM_002187.3:c.618G= MANE Select NP_002178.2:p.Leu206=