Canonical Allele Identifier: CA1595020088
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159326992C= , CM000667.2:g.159326992C= GRCh38
NC_000005.9:g.158754000C= , CM000667.1:g.158754000C= GRCh37
NC_000005.8:g.158686578C= NCBI36
NG_009618.1:g.8482G= , LRG_71:g.8482G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3440G= ENSP00000512849.1:n.-149+3440G=
ENST00000696751.1:c.1-210G= ENSP00000512850.1:n.1-210G=
ENST00000696752.1:n.433-210G=
ENST00000231228.3:c.1-210G= MANE Select ENSP00000231228.2:n.1-210G=
ENST00000231228.2:c.1-210G= ENSP00000231228.2:n.1-210G=
NM_002187.2:c.1-210G= , LRG_71t1:c.1-210G= NP_002178.2:n.1-210G=
NM_002187.3:c.1-210G= MANE Select NP_002178.2:n.1-210G=