Canonical Allele Identifier: CA2676266336
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323027del , CM000667.2:g.159323027del GRCh38
NC_000005.9:g.158750035del , CM000667.1:g.158750035del GRCh37
NC_000005.8:g.158682613del NCBI36
NG_009618.1:g.12448del , LRG_71:g.12448del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2506del ENSP00000512849.1:n.-148-2506del
ENST00000696751.1:c.364+28del ENSP00000512850.1:n.364+28del
ENST00000231228.3:c.364+28del MANE Select ENSP00000231228.2:n.364+28del
ENST00000231228.2:c.364+28del ENSP00000231228.2:n.364+28del
NM_002187.2:c.364+28del , LRG_71t1:c.364+28del NP_002178.2:n.364+28del
XR_001742945.1:n.147+2431del
NM_002187.3:c.364+28del MANE Select NP_002178.2:n.364+28del