Canonical Allele Identifier: CA2676265378
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323442-A-AG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323443dup , CM000667.2:g.159323443dup GRCh38
NC_000005.9:g.158750451dup , CM000667.1:g.158750451dup GRCh37
NC_000005.8:g.158683029dup NCBI36
NG_009618.1:g.12031dup , LRG_71:g.12031dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2923dup ENSP00000512849.1:n.-148-2923dup
ENST00000696751.1:c.89-114dup ENSP00000512850.1:n.89-114dup
ENST00000231228.3:c.89-114dup MANE Select ENSP00000231228.2:n.89-114dup
ENST00000231228.2:c.89-114dup ENSP00000231228.2:n.89-114dup
NM_002187.2:c.89-114dup , LRG_71t1:c.89-114dup NP_002178.2:n.89-114dup
XR_001742945.1:n.148-2091dup
NM_002187.3:c.89-114dup MANE Select NP_002178.2:n.89-114dup
Search 100 bp 5'
Search 100 bp 3'