Canonical Allele Identifier: CA806394997
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1224594339

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327059G>C , CM000667.2:g.159327059G>C GRCh38
NC_000005.9:g.158754067G>C , CM000667.1:g.158754067G>C GRCh37
NC_000005.8:g.158686645G>C NCBI36
NG_009618.1:g.8415C>G , LRG_71:g.8415C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3373C>G ENSP00000512849.1:n.-149+3373C>G
ENST00000696751.1:c.1-277C>G ENSP00000512850.1:n.1-277C>G
ENST00000696752.1:n.433-277C>G
ENST00000231228.3:c.1-277C>G MANE Select ENSP00000231228.2:n.1-277C>G
ENST00000231228.2:c.1-277C>G ENSP00000231228.2:n.1-277C>G
NM_002187.2:c.1-277C>G , LRG_71t1:c.1-277C>G NP_002178.2:n.1-277C>G
NM_002187.3:c.1-277C>G MANE Select NP_002178.2:n.1-277C>G