Canonical Allele Identifier: CA1595045730
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316086A= , CM000667.2:g.159316086A= GRCh38
NC_000005.9:g.158743094A= , CM000667.1:g.158743094A= GRCh37
NC_000005.8:g.158675672A= NCBI36
NG_009618.1:g.19388T= , LRG_71:g.19388T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*15T= ENSP00000512849.1:n.*15T=
ENST00000696751.1:c.*497T= ENSP00000512850.1:n.*497T=
ENST00000231228.3:c.*15T= MANE Select ENSP00000231228.2:n.*15T=
ENST00000231228.2:c.*15T= ENSP00000231228.2:n.*15T=
NM_002187.2:c.*15T= , LRG_71t1:c.*15T= NP_002178.2:n.*15T=
NM_002187.3:c.*15T= MANE Select NP_002178.2:n.*15T=