Canonical Allele Identifier: CA806396137

Gene: IL12B

Linked Data

• dbSNP Id: rs1429690959
• MyVariant Identifiers: chr5:g.158755998_158755999del (hg19) ; chr5:g.159328990_159328991del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328993_159328994del , CM000667.2:g.159328993_159328994del	GRCh38
NC_000005.9:g.158756001_158756002del , CM000667.1:g.158756001_158756002del	GRCh37
NC_000005.8:g.158688579_158688580del	NCBI36
NG_009618.1:g.6483_6484del , LRG_71:g.6483_6484del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1441_-149+1442del	ENSP00000512849.1:n.-149+1441_-149+1442del
ENST00000696751.1:c.-1+1441_-1+1442del	ENSP00000512850.1:n.-1+1441_-1+1442del
ENST00000696752.1:n.432+1441_432+1442del
ENST00000231228.3:c.-1+1441_-1+1442del MANE Select	ENSP00000231228.2:n.-1+1441_-1+1442del
ENST00000231228.2:c.-1+1441_-1+1442del	ENSP00000231228.2:n.-1+1441_-1+1442del
NM_002187.2:c.-1+1441_-1+1442del , LRG_71t1:c.-1+1441_-1+1442del	NP_002178.2:n.-1+1441_-1+1442del
NM_002187.3:c.-1+1441_-1+1442del MANE Select	NP_002178.2:n.-1+1441_-1+1442del