Canonical Allele Identifier: CA2676265284
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323289-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323291del , CM000667.2:g.159323291del GRCh38
NC_000005.9:g.158750299del , CM000667.1:g.158750299del GRCh37
NC_000005.8:g.158682877del NCBI36
NG_009618.1:g.12184del , LRG_71:g.12184del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2770del ENSP00000512849.1:n.-148-2770del
ENST00000696751.1:c.128del ENSP00000512850.1:p.Gly43GlufsTer27
ENST00000231228.3:c.128del MANE Select ENSP00000231228.2:p.Gly43GlufsTer27
ENST00000231228.2:c.128del ENSP00000231228.2:p.Gly43GlufsTer27
NM_002187.2:c.128del , LRG_71t1:c.128del NP_002178.2:p.Gly43GlufsTer27
XR_001742945.1:n.148-2243del
NM_002187.3:c.128del MANE Select NP_002178.2:p.Gly43GlufsTer27
Search 100 bp 5'
Search 100 bp 3'