Canonical Allele Identifier: CA806395078
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1261561047

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327168G>T , CM000667.2:g.159327168G>T GRCh38
NC_000005.9:g.158754176G>T , CM000667.1:g.158754176G>T GRCh37
NC_000005.8:g.158686754G>T NCBI36
NG_009618.1:g.8306C>A , LRG_71:g.8306C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3264C>A ENSP00000512849.1:n.-149+3264C>A
ENST00000696751.1:c.1-386C>A ENSP00000512850.1:n.1-386C>A
ENST00000696752.1:n.433-386C>A
ENST00000231228.3:c.1-386C>A MANE Select ENSP00000231228.2:n.1-386C>A
ENST00000231228.2:c.1-386C>A ENSP00000231228.2:n.1-386C>A
NM_002187.2:c.1-386C>A , LRG_71t1:c.1-386C>A NP_002178.2:n.1-386C>A
NM_002187.3:c.1-386C>A MANE Select NP_002178.2:n.1-386C>A