Canonical Allele Identifier: CA1595018286
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754112107
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322630_159322636del , CM000667.2:g.159322630_159322636del GRCh38
NC_000005.9:g.158749638_158749644del , CM000667.1:g.158749638_158749644del GRCh37
NC_000005.8:g.158682216_158682222del NCBI36
NG_009618.1:g.12838_12844del , LRG_71:g.12838_12844del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2116_-148-2110del ENSP00000512849.1:n.-148-2116_-148-2110del
ENST00000696751.1:c.364+418_364+424del ENSP00000512850.1:n.364+418_364+424del
ENST00000231228.3:c.365-125_365-119del MANE Select ENSP00000231228.2:n.365-125_365-119del
ENST00000231228.2:c.365-125_365-119del ENSP00000231228.2:n.365-125_365-119del
NM_002187.2:c.365-125_365-119del , LRG_71t1:c.365-125_365-119del NP_002178.2:n.365-125_365-119del
XR_001742945.1:n.147+2034_147+2040del
NM_002187.3:c.365-125_365-119del MANE Select NP_002178.2:n.365-125_365-119del
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