Canonical Allele Identifier: CA1595017096

Gene: IL12B

Linked Data

• dbSNP Id: rs1754058699

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159319990G>A , CM000667.2:g.159319990G>A	GRCh38
NC_000005.9:g.158746998G>A , CM000667.1:g.158746998G>A	GRCh37
NC_000005.8:g.158679576G>A	NCBI36
NG_009618.1:g.15484C>T , LRG_71:g.15484C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+316C>T	ENSP00000512849.1:n.67+316C>T
ENST00000696751.1:c.*192+316C>T	ENSP00000512850.1:n.*192+316C>T
ENST00000231228.3:c.697+316C>T MANE Select	ENSP00000231228.2:n.697+316C>T
ENST00000231228.2:c.697+316C>T	ENSP00000231228.2:n.697+316C>T
NM_002187.2:c.697+316C>T , LRG_71t1:c.697+316C>T	NP_002178.2:n.697+316C>T
NM_002187.3:c.697+316C>T MANE Select	NP_002178.2:n.697+316C>T