Canonical Allele Identifier: CA1595020187
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327245G= , CM000667.2:g.159327245G= GRCh38
NC_000005.9:g.158754253G= , CM000667.1:g.158754253G= GRCh37
NC_000005.8:g.158686831G= NCBI36
NG_009618.1:g.8229C= , LRG_71:g.8229C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3187C= ENSP00000512849.1:n.-149+3187C=
ENST00000696751.1:c.1-463C= ENSP00000512850.1:n.1-463C=
ENST00000696752.1:n.433-463C=
ENST00000231228.3:c.1-463C= MANE Select ENSP00000231228.2:n.1-463C=
ENST00000231228.2:c.1-463C= ENSP00000231228.2:n.1-463C=
NM_002187.2:c.1-463C= , LRG_71t1:c.1-463C= NP_002178.2:n.1-463C=
NM_002187.3:c.1-463C= MANE Select NP_002178.2:n.1-463C=