Canonical Allele Identifier: CA362032528
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320368A>C , CM000667.2:g.159320368A>C GRCh38
NC_000005.9:g.158747376A>C , CM000667.1:g.158747376A>C GRCh37
NC_000005.8:g.158679954A>C NCBI36
NG_009618.1:g.15106T>G , LRG_71:g.15106T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.5T>G ENSP00000512849.1:p.Val2Gly
ENST00000696751.1:c.*130T>G ENSP00000512850.1:n.*130T>G
ENST00000231228.3:c.635T>G MANE Select ENSP00000231228.2:p.Val212Gly
ENST00000231228.2:c.635T>G ENSP00000231228.2:p.Val212Gly
NM_002187.2:c.635T>G , LRG_71t1:c.635T>G NP_002178.2:p.Val212Gly
NM_002187.3:c.635T>G MANE Select NP_002178.2:p.Val212Gly