Canonical Allele Identifier: CA362032519
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320366C>G , CM000667.2:g.159320366C>G GRCh38
NC_000005.9:g.158747374C>G , CM000667.1:g.158747374C>G GRCh37
NC_000005.8:g.158679952C>G NCBI36
NG_009618.1:g.15108G>C , LRG_71:g.15108G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.7G>C ENSP00000512849.1:p.Asp3His
ENST00000696751.1:c.*132G>C ENSP00000512850.1:n.*132G>C
ENST00000231228.3:c.637G>C MANE Select ENSP00000231228.2:p.Asp213His
ENST00000231228.2:c.637G>C ENSP00000231228.2:p.Asp213His
NM_002187.2:c.637G>C , LRG_71t1:c.637G>C NP_002178.2:p.Asp213His
NM_002187.3:c.637G>C MANE Select NP_002178.2:p.Asp213His