Canonical Allele Identifier: CA1595018431

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323004_159323005delinsCT , CM000667.2:g.159323004_159323005delinsCT	GRCh38
NC_000005.9:g.158750012_158750013delinsCT , CM000667.1:g.158750012_158750013delinsCT	GRCh37
NC_000005.8:g.158682590_158682591delinsCT	NCBI36
NG_009618.1:g.12469_12470delinsAG , LRG_71:g.12469_12470delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2485_-148-2484delinsAG	ENSP00000512849.1:n.-148-2485_-148-2484delinsAG
ENST00000696751.1:c.364+49_364+50delinsAG	ENSP00000512850.1:n.364+49_364+50delinsAG
ENST00000231228.3:c.364+49_364+50delinsAG MANE Select	ENSP00000231228.2:n.364+49_364+50delinsAG
ENST00000231228.2:c.364+49_364+50delinsAG	ENSP00000231228.2:n.364+49_364+50delinsAG
NM_002187.2:c.364+49_364+50delinsAG , LRG_71t1:c.364+49_364+50delinsAG	NP_002178.2:n.364+49_364+50delinsAG
XR_001742945.1:n.147+2408_147+2409delinsCT
NM_002187.3:c.364+49_364+50delinsAG MANE Select	NP_002178.2:n.364+49_364+50delinsAG