Canonical Allele Identifier: CA3538788
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs781239114

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320567A>T , CM000667.2:g.159320567A>T GRCh38
NC_000005.9:g.158747575A>T , CM000667.1:g.158747575A>T GRCh37
NC_000005.8:g.158680153A>T NCBI36
NG_009618.1:g.14907T>A , LRG_71:g.14907T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-47T>A ENSP00000512849.1:n.-148-47T>A
ENST00000696751.1:c.365-47T>A ENSP00000512850.1:n.365-47T>A
ENST00000231228.3:c.483-47T>A MANE Select ENSP00000231228.2:n.483-47T>A
ENST00000231228.2:c.483-47T>A ENSP00000231228.2:n.483-47T>A
NM_002187.2:c.483-47T>A , LRG_71t1:c.483-47T>A NP_002178.2:n.483-47T>A
XR_001742945.1:n.118A>T
NM_002187.3:c.483-47T>A MANE Select NP_002178.2:n.483-47T>A