Canonical Allele Identifier: CA1595017353
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754070239
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320567_159320568del , CM000667.2:g.159320567_159320568del GRCh38
NC_000005.9:g.158747575_158747576del , CM000667.1:g.158747575_158747576del GRCh37
NC_000005.8:g.158680153_158680154del NCBI36
NG_009618.1:g.14911_14912del , LRG_71:g.14911_14912del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-43_-148-42del ENSP00000512849.1:n.-148-43_-148-42del
ENST00000696751.1:c.365-43_365-42del ENSP00000512850.1:n.365-43_365-42del
ENST00000231228.3:c.483-43_483-42del MANE Select ENSP00000231228.2:n.483-43_483-42del
ENST00000231228.2:c.483-43_483-42del ENSP00000231228.2:n.483-43_483-42del
NM_002187.2:c.483-43_483-42del , LRG_71t1:c.483-43_483-42del NP_002178.2:n.483-43_483-42del
XR_001742945.1:n.118_119del
NM_002187.3:c.483-43_483-42del MANE Select NP_002178.2:n.483-43_483-42del
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