Canonical Allele Identifier: CA2676264556
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315948del , CM000667.2:g.159315948del GRCh38
NC_000005.9:g.158742956del , CM000667.1:g.158742956del GRCh37
NC_000005.8:g.158675534del NCBI36
NG_009618.1:g.19526del , LRG_71:g.19526del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*153del ENSP00000512849.1:n.*153del
ENST00000696751.1:c.*635del ENSP00000512850.1:n.*635del
ENST00000231228.3:c.*153del MANE Select ENSP00000231228.2:n.*153del
ENST00000231228.2:c.*153del ENSP00000231228.2:n.*153del
NM_002187.2:c.*153del , LRG_71t1:c.*153del NP_002178.2:n.*153del
NM_002187.3:c.*153del MANE Select NP_002178.2:n.*153del