Canonical Allele Identifier: CA2984324926

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322078_159322080del , CM000667.2:g.159322078_159322080del	GRCh38
NC_000005.9:g.158749086_158749088del , CM000667.1:g.158749086_158749088del	GRCh37
NC_000005.8:g.158681664_158681666del	NCBI36
NG_009618.1:g.13394_13396del , LRG_71:g.13394_13396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1560_-148-1558del	ENSP00000512849.1:n.-148-1560_-148-1558del
ENST00000696751.1:c.364+974_364+976del	ENSP00000512850.1:n.364+974_364+976del
ENST00000231228.3:c.482+314_482+316del MANE Select	ENSP00000231228.2:n.482+314_482+316del
ENST00000231228.2:c.482+314_482+316del	ENSP00000231228.2:n.482+314_482+316del
NM_002187.2:c.482+314_482+316del , LRG_71t1:c.482+314_482+316del	NP_002178.2:n.482+314_482+316del
XR_001742945.1:n.147+1482_147+1484del
NM_002187.3:c.482+314_482+316del MANE Select	NP_002178.2:n.482+314_482+316del