Canonical Allele Identifier: CA806389195
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1429026228
MyVariant Identifiers: chr5:g.158747030del (hg19) chr5:g.159320022del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320022del , CM000667.2:g.159320022del GRCh38
NC_000005.9:g.158747030del , CM000667.1:g.158747030del GRCh37
NC_000005.8:g.158679608del NCBI36
NG_009618.1:g.15452del , LRG_71:g.15452del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+284del ENSP00000512849.1:n.67+284del
ENST00000696751.1:c.*192+284del ENSP00000512850.1:n.*192+284del
ENST00000231228.3:c.697+284del MANE Select ENSP00000231228.2:n.697+284del
ENST00000231228.2:c.697+284del ENSP00000231228.2:n.697+284del
NM_002187.2:c.697+284del , LRG_71t1:c.697+284del NP_002178.2:n.697+284del
NM_002187.3:c.697+284del MANE Select NP_002178.2:n.697+284del
Search 100 bp 5'
Search 100 bp 3'