Canonical Allele Identifier: CA1595020184

Gene: IL12B

Linked Data

• dbSNP Id: rs1754206575

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327231_159327233dup , CM000667.2:g.159327231_159327233dup	GRCh38
NC_000005.9:g.158754239_158754241dup , CM000667.1:g.158754239_158754241dup	GRCh37
NC_000005.8:g.158686817_158686819dup	NCBI36
NG_009618.1:g.8241_8243dup , LRG_71:g.8241_8243dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+3199_-149+3201dup	ENSP00000512849.1:n.-149+3199_-149+3201du...
ENST00000696751.1:c.1-451_1-449dup	ENSP00000512850.1:n.1-451_1-449dup
ENST00000696752.1:n.433-451_433-449dup
ENST00000231228.3:c.1-451_1-449dup MANE Select	ENSP00000231228.2:n.1-451_1-449dup
ENST00000231228.2:c.1-451_1-449dup	ENSP00000231228.2:n.1-451_1-449dup
NM_002187.2:c.1-451_1-449dup , LRG_71t1:c.1-451_1-449dup	NP_002178.2:n.1-451_1-449dup
NM_002187.3:c.1-451_1-449dup MANE Select	NP_002178.2:n.1-451_1-449dup