Canonical Allele Identifier: CA2676264242
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315020C>A , CM000667.2:g.159315020C>A GRCh38
NC_000005.9:g.158742028C>A , CM000667.1:g.158742028C>A GRCh37
NC_000005.8:g.158674606C>A NCBI36
NG_009618.1:g.20454G>T , LRG_71:g.20454G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1081G>T ENSP00000512849.1:n.*1081G>T
ENST00000696751.1:c.*1563G>T ENSP00000512850.1:n.*1563G>T
ENST00000231228.3:c.*1081G>T MANE Select ENSP00000231228.2:n.*1081G>T
ENST00000231228.2:c.*1081G>T ENSP00000231228.2:n.*1081G>T
NM_002187.2:c.*1081G>T , LRG_71t1:c.*1081G>T NP_002178.2:n.*1081G>T
XR_941138.1:n.364-198C>A
XR_941138.2:n.431-198C>A
NM_002187.3:c.*1081G>T MANE Select NP_002178.2:n.*1081G>T