Canonical Allele Identifier: CA806427971
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1304593123
gnomAD v3: 5-159315981-AAAAAACGTT-A
gnomAD v4: 5-159315981-AAAAAACGTT-A
MyVariant Identifiers: chr5:g.158742990_158742998del (hg19) chr5:g.159315982_159315990del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315982_159315990del , CM000667.2:g.159315982_159315990del GRCh38
NC_000005.9:g.158742990_158742998del , CM000667.1:g.158742990_158742998del GRCh37
NC_000005.8:g.158675568_158675576del NCBI36
NG_009618.1:g.19484_19492del , LRG_71:g.19484_19492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*111_*119del ENSP00000512849.1:n.*111_*119del
ENST00000696751.1:c.*593_*601del ENSP00000512850.1:n.*593_*601del
ENST00000231228.3:c.*111_*119del MANE Select ENSP00000231228.2:n.*111_*119del
ENST00000231228.2:c.*111_*119del ENSP00000231228.2:n.*111_*119del
NM_002187.2:c.*111_*119del , LRG_71t1:c.*111_*119del NP_002178.2:n.*111_*119del
NM_002187.3:c.*111_*119del MANE Select NP_002178.2:n.*111_*119del
Search 100 bp 5'
Search 100 bp 3'