Canonical Allele Identifier: CA2676264531
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315910_159315911del , CM000667.2:g.159315910_159315911del GRCh38
NC_000005.9:g.158742918_158742919del , CM000667.1:g.158742918_158742919del GRCh37
NC_000005.8:g.158675496_158675497del NCBI36
NG_009618.1:g.19563_19564del , LRG_71:g.19563_19564del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*190_*191del ENSP00000512849.1:n.*190_*191del
ENST00000696751.1:c.*672_*673del ENSP00000512850.1:n.*672_*673del
ENST00000231228.3:c.*190_*191del MANE Select ENSP00000231228.2:n.*190_*191del
ENST00000231228.2:c.*190_*191del ENSP00000231228.2:n.*190_*191del
NM_002187.2:c.*190_*191del , LRG_71t1:c.*190_*191del NP_002178.2:n.*190_*191del
NM_002187.3:c.*190_*191del MANE Select NP_002178.2:n.*190_*191del