Canonical Allele Identifier: CA129827037
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs757477829

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320572C>T , CM000667.2:g.159320572C>T GRCh38
NC_000005.9:g.158747580C>T , CM000667.1:g.158747580C>T GRCh37
NC_000005.8:g.158680158C>T NCBI36
NG_009618.1:g.14902G>A , LRG_71:g.14902G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000231228.3:c.483-52G>A MANE Select ENSP00000231228.2:p.=
ENST00000231228.2:c.483-52G>A ENSP00000231228.2:p.=
NM_002187.2:c.483-52G>A , LRG_71t1:c.483-52G>A NP_002178.2:p.=
XR_001742945.1:n.123C>T
NM_002187.3:c.483-52G>A MANE Select NP_002178.2:p.=