Canonical Allele Identifier: CA129831460
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs536424729

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327176T>C , CM000667.2:g.159327176T>C GRCh38
NC_000005.9:g.158754184T>C , CM000667.1:g.158754184T>C GRCh37
NC_000005.8:g.158686762T>C NCBI36
NG_009618.1:g.8298A>G , LRG_71:g.8298A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3256A>G ENSP00000512849.1:n.-149+3256A>G
ENST00000696751.1:c.1-394A>G ENSP00000512850.1:n.1-394A>G
ENST00000696752.1:n.433-394A>G
ENST00000231228.3:c.1-394A>G MANE Select ENSP00000231228.2:n.1-394A>G
ENST00000231228.2:c.1-394A>G ENSP00000231228.2:n.1-394A>G
NM_002187.2:c.1-394A>G , LRG_71t1:c.1-394A>G NP_002178.2:n.1-394A>G
NM_002187.3:c.1-394A>G MANE Select NP_002178.2:n.1-394A>G