Canonical Allele Identifier: CA1595017354
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320562_159320563delinsGA , CM000667.2:g.159320562_159320563delinsGA GRCh38
NC_000005.9:g.158747570_158747571delinsGA , CM000667.1:g.158747570_158747571delinsGA GRCh37
NC_000005.8:g.158680148_158680149delinsGA NCBI36
NG_009618.1:g.14911_14912delinsTC , LRG_71:g.14911_14912delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-43_-148-42delinsTC ENSP00000512849.1:n.-148-43_-148-42delins...
ENST00000696751.1:c.365-43_365-42delinsTC ENSP00000512850.1:n.365-43_365-42delinsTC...
ENST00000231228.3:c.483-43_483-42delinsTC MANE Select ENSP00000231228.2:n.483-43_483-42delinsTC...
ENST00000231228.2:c.483-43_483-42delinsTC ENSP00000231228.2:n.483-43_483-42delinsTC...
NM_002187.2:c.483-43_483-42delinsTC , LRG_71t1:c.483-43_483-42delinsTC NP_002178.2:n.483-43_483-42delinsTC
XR_001742945.1:n.113_114delinsGA
NM_002187.3:c.483-43_483-42delinsTC MANE Select NP_002178.2:n.483-43_483-42delinsTC