Canonical Allele Identifier: CA1595020128

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327092_159327093delinsAT , CM000667.2:g.159327092_159327093delinsAT	GRCh38
NC_000005.9:g.158754100_158754101delinsAT , CM000667.1:g.158754100_158754101delinsAT	GRCh37
NC_000005.8:g.158686678_158686679delinsAT	NCBI36
NG_009618.1:g.8381_8382delinsAT , LRG_71:g.8381_8382delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+3339_-149+3340delinsAT	ENSP00000512849.1:n.-149+3339_-149+3340de...
ENST00000696751.1:c.1-311_1-310delinsAT	ENSP00000512850.1:n.1-311_1-310delinsAT
ENST00000696752.1:n.433-311_433-310delinsAT
ENST00000231228.3:c.1-311_1-310delinsAT MANE Select	ENSP00000231228.2:n.1-311_1-310delinsAT
ENST00000231228.2:c.1-311_1-310delinsAT	ENSP00000231228.2:n.1-311_1-310delinsAT
NM_002187.2:c.1-311_1-310delinsAT , LRG_71t1:c.1-311_1-310delinsAT	NP_002178.2:n.1-311_1-310delinsAT
NM_002187.3:c.1-311_1-310delinsAT MANE Select	NP_002178.2:n.1-311_1-310delinsAT