Canonical Allele Identifier: CA2676264535
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315918_159315923del , CM000667.2:g.159315918_159315923del GRCh38
NC_000005.9:g.158742926_158742931del , CM000667.1:g.158742926_158742931del GRCh37
NC_000005.8:g.158675504_158675509del NCBI36
NG_009618.1:g.19551_19556del , LRG_71:g.19551_19556del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*178_*183del ENSP00000512849.1:n.*178_*183del
ENST00000696751.1:c.*660_*665del ENSP00000512850.1:n.*660_*665del
ENST00000231228.3:c.*178_*183del MANE Select ENSP00000231228.2:n.*178_*183del
ENST00000231228.2:c.*178_*183del ENSP00000231228.2:n.*178_*183del
NM_002187.2:c.*178_*183del , LRG_71t1:c.*178_*183del NP_002178.2:n.*178_*183del
NM_002187.3:c.*178_*183del MANE Select NP_002178.2:n.*178_*183del