Canonical Allele Identifier: CA362032498
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320362G>C , CM000667.2:g.159320362G>C GRCh38
NC_000005.9:g.158747370G>C , CM000667.1:g.158747370G>C GRCh37
NC_000005.8:g.158679948G>C NCBI36
NG_009618.1:g.15112C>G , LRG_71:g.15112C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.11C>G ENSP00000512849.1:p.Ala4Gly
ENST00000696751.1:c.*136C>G ENSP00000512850.1:n.*136C>G
ENST00000231228.3:c.641C>G MANE Select ENSP00000231228.2:p.Ala214Gly
ENST00000231228.2:c.641C>G ENSP00000231228.2:p.Ala214Gly
NM_002187.2:c.641C>G , LRG_71t1:c.641C>G NP_002178.2:p.Ala214Gly
NM_002187.3:c.641C>G MANE Select NP_002178.2:p.Ala214Gly