Canonical Allele Identifier: CA1595017993

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321914_159321917delinsTCAG , CM000667.2:g.159321914_159321917delinsTCAG	GRCh38
NC_000005.9:g.158748922_158748925delinsTCAG , CM000667.1:g.158748922_158748925delinsTCAG	GRCh37
NC_000005.8:g.158681500_158681503delinsTCAG	NCBI36
NG_009618.1:g.13557_13560delinsCTGA , LRG_71:g.13557_13560delinsCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1397_-148-1394delinsCTGA	ENSP00000512849.1:n.-148-1397_-148-1394delinsCTGA
ENST00000696751.1:c.364+1137_364+1140delinsCTGA	ENSP00000512850.1:n.364+1137_364+1140delinsCTGA
ENST00000231228.3:c.482+477_482+480delinsCTGA MANE Select	ENSP00000231228.2:n.482+477_482+480delinsCTGA
ENST00000231228.2:c.482+477_482+480delinsCTGA	ENSP00000231228.2:n.482+477_482+480delinsCTGA
NM_002187.2:c.482+477_482+480delinsCTGA , LRG_71t1:c.482+477_482+480delinsCTGA	NP_002178.2:n.482+477_482+480delinsCTGA
XR_001742945.1:n.147+1318_147+1321delinsTCAG
NM_002187.3:c.482+477_482+480delinsCTGA MANE Select	NP_002178.2:n.482+477_482+480delinsCTGA