Canonical Allele Identifier: CA806427977
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1440481384

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316006_159316009del , CM000667.2:g.159316006_159316009del GRCh38
NC_000005.9:g.158743014_158743017del , CM000667.1:g.158743014_158743017del GRCh37
NC_000005.8:g.158675592_158675595del NCBI36
NG_009618.1:g.19468_19471del , LRG_71:g.19468_19471del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*95_*98del ENSP00000512849.1:n.*95_*98del
ENST00000696751.1:c.*577_*580del ENSP00000512850.1:n.*577_*580del
ENST00000231228.3:c.*95_*98del MANE Select ENSP00000231228.2:n.*95_*98del
ENST00000231228.2:c.*95_*98del ENSP00000231228.2:n.*95_*98del
NM_002187.2:c.*95_*98del , LRG_71t1:c.*95_*98del NP_002178.2:n.*95_*98del
NM_002187.3:c.*95_*98del MANE Select NP_002178.2:n.*95_*98del