Canonical Allele Identifier: CA362036934
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323300C>A , CM000667.2:g.159323300C>A GRCh38
NC_000005.9:g.158750308C>A , CM000667.1:g.158750308C>A GRCh37
NC_000005.8:g.158682886C>A NCBI36
NG_009618.1:g.12174G>T , LRG_71:g.12174G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2780G>T ENSP00000512849.1:n.-148-2780G>T
ENST00000696751.1:c.118G>T ENSP00000512850.1:p.Asp40Tyr
ENST00000231228.3:c.118G>T MANE Select ENSP00000231228.2:p.Asp40Tyr
ENST00000231228.2:c.118G>T ENSP00000231228.2:p.Asp40Tyr
NM_002187.2:c.118G>T , LRG_71t1:c.118G>T NP_002178.2:p.Asp40Tyr
XR_001742945.1:n.148-2234C>A
NM_002187.3:c.118G>T MANE Select NP_002178.2:p.Asp40Tyr