Canonical Allele Identifier: CA1595017343

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320545_159320547delinsCTG , CM000667.2:g.159320545_159320547delinsCTG	GRCh38
NC_000005.9:g.158747553_158747555delinsCTG , CM000667.1:g.158747553_158747555delinsCTG	GRCh37
NC_000005.8:g.158680131_158680133delinsCTG	NCBI36
NG_009618.1:g.14927_14929delinsCAG , LRG_71:g.14927_14929delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-27_-148-25delinsCAG	ENSP00000512849.1:n.-148-27_-148-25delinsCAG
ENST00000696751.1:c.365-27_365-25delinsCAG	ENSP00000512850.1:n.365-27_365-25delinsCAG
ENST00000231228.3:c.483-27_483-25delinsCAG MANE Select	ENSP00000231228.2:n.483-27_483-25delinsCAG
ENST00000231228.2:c.483-27_483-25delinsCAG	ENSP00000231228.2:n.483-27_483-25delinsCAG
NM_002187.2:c.483-27_483-25delinsCAG , LRG_71t1:c.483-27_483-25delinsCAG	NP_002178.2:n.483-27_483-25delinsCAG
XR_001742945.1:n.96_98delinsCTG
NM_002187.3:c.483-27_483-25delinsCAG MANE Select	NP_002178.2:n.483-27_483-25delinsCAG