Canonical Allele Identifier: CA1595020226

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327351_159327353delinsAGT , CM000667.2:g.159327351_159327353delinsAGT	GRCh38
NC_000005.9:g.158754359_158754361delinsAGT , CM000667.1:g.158754359_158754361delinsAGT	GRCh37
NC_000005.8:g.158686937_158686939delinsAGT	NCBI36
NG_009618.1:g.8121_8123delinsACT , LRG_71:g.8121_8123delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3079_-149+3081delinsACT	ENSP00000512849.1:n.-149+3079_-149+3081delinsACT
ENST00000696751.1:c.1-571_1-569delinsACT	ENSP00000512850.1:n.1-571_1-569delinsACT
ENST00000696752.1:n.433-571_433-569delinsACT
ENST00000231228.3:c.1-571_1-569delinsACT MANE Select	ENSP00000231228.2:n.1-571_1-569delinsACT
ENST00000231228.2:c.1-571_1-569delinsACT	ENSP00000231228.2:n.1-571_1-569delinsACT
NM_002187.2:c.1-571_1-569delinsACT , LRG_71t1:c.1-571_1-569delinsACT	NP_002178.2:n.1-571_1-569delinsACT
NM_002187.3:c.1-571_1-569delinsACT MANE Select	NP_002178.2:n.1-571_1-569delinsACT