Canonical Allele Identifier: CA1595045773
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316189T= , CM000667.2:g.159316189T= GRCh38
NC_000005.9:g.158743197T= , CM000667.1:g.158743197T= GRCh37
NC_000005.8:g.158675775T= NCBI36
NG_009618.1:g.19285A= , LRG_71:g.19285A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1-89A= ENSP00000512849.1:n.*1-89A=
ENST00000696751.1:c.*483-89A= ENSP00000512850.1:n.*483-89A=
ENST00000231228.3:c.*1-89A= MANE Select ENSP00000231228.2:n.*1-89A=
ENST00000231228.2:c.*1-89A= ENSP00000231228.2:n.*1-89A=
NM_002187.2:c.*1-89A= , LRG_71t1:c.*1-89A= NP_002178.2:n.*1-89A=
NM_002187.3:c.*1-89A= MANE Select NP_002178.2:n.*1-89A=