Canonical Allele Identifier: CA2710491881

Gene: IL12B

Linked Data

• dbSNP Id: rs2113028282

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321991_159321993dup , CM000667.2:g.159321991_159321993dup	GRCh38
NC_000005.9:g.158748999_158749001dup , CM000667.1:g.158748999_158749001dup	GRCh37
NC_000005.8:g.158681577_158681579dup	NCBI36
NG_009618.1:g.13481_13483dup , LRG_71:g.13481_13483dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1473_-148-1471dup	ENSP00000512849.1:n.-148-1473_-148-1471dup
ENST00000696751.1:c.364+1061_364+1063dup	ENSP00000512850.1:n.364+1061_364+1063dup
ENST00000231228.3:c.482+401_482+403dup MANE Select	ENSP00000231228.2:n.482+401_482+403dup
ENST00000231228.2:c.482+401_482+403dup	ENSP00000231228.2:n.482+401_482+403dup
NM_002187.2:c.482+401_482+403dup , LRG_71t1:c.482+401_482+403dup	NP_002178.2:n.482+401_482+403dup
XR_001742945.1:n.147+1395_147+1397dup
NM_002187.3:c.482+401_482+403dup MANE Select	NP_002178.2:n.482+401_482+403dup