Canonical Allele Identifier: CA1595018487
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323112_159323120delinsCAGGAGCGA , CM000667.2:g.159323112_159323120delinsCAGGAGCGA GRCh38
NC_000005.9:g.158750120_158750128delinsCAGGAGCGA , CM000667.1:g.158750120_158750128delinsCAGGAGCGA GRCh37
NC_000005.8:g.158682698_158682706delinsCAGGAGCGA NCBI36
NG_009618.1:g.12354_12362delinsTCGCTCCTG , LRG_71:g.12354_12362delinsTCGCTCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2600_-148-2592delinsTCGCTCCTG ENSP00000512849.1:n.-148-2600_-148-2592de...
ENST00000696751.1:c.298_306delinsTCGCTCCTG ENSP00000512850.1:p.Ser100=
ENST00000231228.3:c.298_306delinsTCGCTCCTG MANE Select ENSP00000231228.2:p.Ser100=
ENST00000231228.2:c.298_306delinsTCGCTCCTG ENSP00000231228.2:p.Ser100=
NM_002187.2:c.298_306delinsTCGCTCCTG , LRG_71t1:c.298_306delinsTCGCTCCTG NP_002178.2:p.Ser100=
XR_001742945.1:n.148-2422_148-2414delinsCAGGAGCGA
NM_002187.3:c.298_306delinsTCGCTCCTG MANE Select NP_002178.2:p.Ser100=