Canonical Allele Identifier: CA1595020236

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327385_159327388delinsGGGT , CM000667.2:g.159327385_159327388delinsGGGT	GRCh38
NC_000005.9:g.158754393_158754396delinsGGGT , CM000667.1:g.158754393_158754396delinsGGGT	GRCh37
NC_000005.8:g.158686971_158686974delinsGGGT	NCBI36
NG_009618.1:g.8086_8089delinsACCC , LRG_71:g.8086_8089delinsACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3044_-149+3047delinsACCC	ENSP00000512849.1:n.-149+3044_-149+3047delinsACCC
ENST00000696751.1:c.1-606_1-603delinsACCC	ENSP00000512850.1:n.1-606_1-603delinsACCC
ENST00000696752.1:n.433-606_433-603delinsACCC
ENST00000231228.3:c.1-606_1-603delinsACCC MANE Select	ENSP00000231228.2:n.1-606_1-603delinsACCC
ENST00000231228.2:c.1-606_1-603delinsACCC	ENSP00000231228.2:n.1-606_1-603delinsACCC
NM_002187.2:c.1-606_1-603delinsACCC , LRG_71t1:c.1-606_1-603delinsACCC	NP_002178.2:n.1-606_1-603delinsACCC
NM_002187.3:c.1-606_1-603delinsACCC MANE Select	NP_002178.2:n.1-606_1-603delinsACCC