Canonical Allele Identifier: CA129826517
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs780279002
gnomAD v2: 5-158747057-GCTGTAGTGGAGTGGAT-G
gnomAD v3: 5-159320049-GCTGTAGTGGAGTGGAT-G
gnomAD v4: 5-159320049-GCTGTAGTGGAGTGGAT-G
MyVariant Identifiers: chr5:g.158747058_158747073del (hg19) chr5:g.159320050_159320065del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320053_159320068del , CM000667.2:g.159320053_159320068del GRCh38
NC_000005.9:g.158747061_158747076del , CM000667.1:g.158747061_158747076del GRCh37
NC_000005.8:g.158679639_158679654del NCBI36
NG_009618.1:g.15409_15424del , LRG_71:g.15409_15424del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+241_67+256del ENSP00000512849.1:n.67+241_67+256del
ENST00000696751.1:c.*192+241_*192+256del ENSP00000512850.1:n.*192+241_*192+256del
ENST00000231228.3:c.697+241_697+256del MANE Select ENSP00000231228.2:n.697+241_697+256del
ENST00000231228.2:c.697+241_697+256del ENSP00000231228.2:n.697+241_697+256del
NM_002187.2:c.697+241_697+256del , LRG_71t1:c.697+241_697+256del NP_002178.2:n.697+241_697+256del
NM_002187.3:c.697+241_697+256del MANE Select NP_002178.2:n.697+241_697+256del
Search 100 bp 5'
Search 100 bp 3'