Canonical Allele Identifier: CA129826525
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs56010741
gnomAD v2: 5-158747075-TG-T
gnomAD v3: 5-159320067-TG-T
gnomAD v4: 5-159320067-TG-T
MyVariant Identifiers: chr5:g.158747076del (hg19) chr5:g.159320068del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320069del , CM000667.2:g.159320069del GRCh38
NC_000005.9:g.158747077del , CM000667.1:g.158747077del GRCh37
NC_000005.8:g.158679655del NCBI36
NG_009618.1:g.15406del , LRG_71:g.15406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+238del ENSP00000512849.1:n.67+238del
ENST00000696751.1:c.*192+238del ENSP00000512850.1:n.*192+238del
ENST00000231228.3:c.697+238del MANE Select ENSP00000231228.2:n.697+238del
ENST00000231228.2:c.697+238del ENSP00000231228.2:n.697+238del
NM_002187.2:c.697+238del , LRG_71t1:c.697+238del NP_002178.2:n.697+238del
NM_002187.3:c.697+238del MANE Select NP_002178.2:n.697+238del
Search 100 bp 5'
Search 100 bp 3'