Canonical Allele Identifier: CA362032550
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320372T>C , CM000667.2:g.159320372T>C GRCh38
NC_000005.9:g.158747380T>C , CM000667.1:g.158747380T>C GRCh37
NC_000005.8:g.158679958T>C NCBI36
NG_009618.1:g.15102A>G , LRG_71:g.15102A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.1A>G ENSP00000512849.1:p.Met1Val
ENST00000696751.1:c.*126A>G ENSP00000512850.1:n.*126A>G
ENST00000231228.3:c.631A>G MANE Select ENSP00000231228.2:p.Met211Val
ENST00000231228.2:c.631A>G ENSP00000231228.2:p.Met211Val
NM_002187.2:c.631A>G , LRG_71t1:c.631A>G NP_002178.2:p.Met211Val
NM_002187.3:c.631A>G MANE Select NP_002178.2:p.Met211Val