Canonical Allele Identifier: CA1595017280
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320382G= , CM000667.2:g.159320382G= GRCh38
NC_000005.9:g.158747390G= , CM000667.1:g.158747390G= GRCh37
NC_000005.8:g.158679968G= NCBI36
NG_009618.1:g.15092C= , LRG_71:g.15092C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-10C= ENSP00000512849.1:n.-10C=
ENST00000696751.1:c.*116C= ENSP00000512850.1:n.*116C=
ENST00000231228.3:c.621C= MANE Select ENSP00000231228.2:p.Pro207=
ENST00000231228.2:c.621C= ENSP00000231228.2:p.Pro207=
NM_002187.2:c.621C= , LRG_71t1:c.621C= NP_002178.2:p.Pro207=
NM_002187.3:c.621C= MANE Select NP_002178.2:p.Pro207=