Canonical Allele Identifier: CA2676265816
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159326917_159326919del , CM000667.2:g.159326917_159326919del GRCh38
NC_000005.9:g.158753925_158753927del , CM000667.1:g.158753925_158753927del GRCh37
NC_000005.8:g.158686503_158686505del NCBI36
NG_009618.1:g.8555_8557del , LRG_71:g.8555_8557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+3513_-149+3515del ENSP00000512849.1:n.-149+3513_-149+3515del
ENST00000696751.1:c.1-137_1-135del ENSP00000512850.1:n.1-137_1-135del
ENST00000696752.1:n.433-137_433-135del
ENST00000231228.3:c.1-137_1-135del MANE Select ENSP00000231228.2:n.1-137_1-135del
ENST00000231228.2:c.1-137_1-135del ENSP00000231228.2:n.1-137_1-135del
NM_002187.2:c.1-137_1-135del , LRG_71t1:c.1-137_1-135del NP_002178.2:n.1-137_1-135del
NM_002187.3:c.1-137_1-135del MANE Select NP_002178.2:n.1-137_1-135del