Canonical Allele Identifier: CA806391615
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1286954415
MyVariant Identifiers: chr5:g.158749853_158749892del (hg19) chr5:g.159322845_159322884del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322848_159322887del , CM000667.2:g.159322848_159322887del GRCh38
NC_000005.9:g.158749856_158749895del , CM000667.1:g.158749856_158749895del GRCh37
NC_000005.8:g.158682434_158682473del NCBI36
NG_009618.1:g.12590_12629del , LRG_71:g.12590_12629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2364_-148-2325del ENSP00000512849.1:n.-148-2364_-148-2325del
ENST00000696751.1:c.364+170_364+209del ENSP00000512850.1:n.364+170_364+209del
ENST00000231228.3:c.364+170_364+209del MANE Select ENSP00000231228.2:n.364+170_364+209del
ENST00000231228.2:c.364+170_364+209del ENSP00000231228.2:n.364+170_364+209del
NM_002187.2:c.364+170_364+209del , LRG_71t1:c.364+170_364+209del NP_002178.2:n.364+170_364+209del
XR_001742945.1:n.147+2252_147+2291del
NM_002187.3:c.364+170_364+209del MANE Select NP_002178.2:n.364+170_364+209del
Search 100 bp 5'
Search 100 bp 3'