Canonical Allele Identifier: CA2676265374
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323436-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323437del , CM000667.2:g.159323437del GRCh38
NC_000005.9:g.158750445del , CM000667.1:g.158750445del GRCh37
NC_000005.8:g.158683023del NCBI36
NG_009618.1:g.12037del , LRG_71:g.12037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2917del ENSP00000512849.1:n.-148-2917del
ENST00000696751.1:c.89-108del ENSP00000512850.1:n.89-108del
ENST00000231228.3:c.89-108del MANE Select ENSP00000231228.2:n.89-108del
ENST00000231228.2:c.89-108del ENSP00000231228.2:n.89-108del
NM_002187.2:c.89-108del , LRG_71t1:c.89-108del NP_002178.2:n.89-108del
XR_001742945.1:n.148-2097del
NM_002187.3:c.89-108del MANE Select NP_002178.2:n.89-108del
Search 100 bp 5'
Search 100 bp 3'