Canonical Allele Identifier: CA362032933
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320464A>G , CM000667.2:g.159320464A>G GRCh38
NC_000005.9:g.158747472A>G , CM000667.1:g.158747472A>G GRCh37
NC_000005.8:g.158680050A>G NCBI36
NG_009618.1:g.15010T>C , LRG_71:g.15010T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-92T>C ENSP00000512849.1:n.-92T>C
ENST00000696751.1:c.*34T>C ENSP00000512850.1:n.*34T>C
ENST00000231228.3:c.539T>C MANE Select ENSP00000231228.2:p.Val180Ala
ENST00000231228.2:c.539T>C ENSP00000231228.2:p.Val180Ala
NM_002187.2:c.539T>C , LRG_71t1:c.539T>C NP_002178.2:p.Val180Ala
XR_001742945.1:n.15A>G
NM_002187.3:c.539T>C MANE Select NP_002178.2:p.Val180Ala