Canonical Allele Identifier: CA3538785
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs373540096

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320557T>C , CM000667.2:g.159320557T>C GRCh38
NC_000005.9:g.158747565T>C , CM000667.1:g.158747565T>C GRCh37
NC_000005.8:g.158680143T>C NCBI36
NG_009618.1:g.14917A>G , LRG_71:g.14917A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000231228.3:c.483-37A>G MANE Select ENSP00000231228.2:p.=
ENST00000231228.2:c.483-37A>G ENSP00000231228.2:p.=
NM_002187.2:c.483-37A>G , LRG_71t1:c.483-37A>G NP_002178.2:p.=
XR_001742945.1:n.108T>C
NM_002187.3:c.483-37A>G MANE Select NP_002178.2:p.=