Canonical Allele Identifier: CA1595045777
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316200G= , CM000667.2:g.159316200G= GRCh38
NC_000005.9:g.158743208G= , CM000667.1:g.158743208G= GRCh37
NC_000005.8:g.158675786G= NCBI36
NG_009618.1:g.19274C= , LRG_71:g.19274C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1-100C= ENSP00000512849.1:n.*1-100C=
ENST00000696751.1:c.*483-100C= ENSP00000512850.1:n.*483-100C=
ENST00000231228.3:c.*1-100C= MANE Select ENSP00000231228.2:n.*1-100C=
ENST00000231228.2:c.*1-100C= ENSP00000231228.2:n.*1-100C=
NM_002187.2:c.*1-100C= , LRG_71t1:c.*1-100C= NP_002178.2:n.*1-100C=
NM_002187.3:c.*1-100C= MANE Select NP_002178.2:n.*1-100C=