Canonical Allele Identifier: CA1595020186
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327237G= , CM000667.2:g.159327237G= GRCh38
NC_000005.9:g.158754245G= , CM000667.1:g.158754245G= GRCh37
NC_000005.8:g.158686823G= NCBI36
NG_009618.1:g.8237C= , LRG_71:g.8237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3195C= ENSP00000512849.1:n.-149+3195C=
ENST00000696751.1:c.1-455C= ENSP00000512850.1:n.1-455C=
ENST00000696752.1:n.433-455C=
ENST00000231228.3:c.1-455C= MANE Select ENSP00000231228.2:n.1-455C=
ENST00000231228.2:c.1-455C= ENSP00000231228.2:n.1-455C=
NM_002187.2:c.1-455C= , LRG_71t1:c.1-455C= NP_002178.2:n.1-455C=
NM_002187.3:c.1-455C= MANE Select NP_002178.2:n.1-455C=