Canonical Allele Identifier: CA2605806755

Gene: IL12B

Linked Data

• gnomAD v3: 5-159328784-CTCAGG-C
• gnomAD v4: 5-159328784-CTCAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328786_159328790del , CM000667.2:g.159328786_159328790del	GRCh38
NC_000005.9:g.158755794_158755798del , CM000667.1:g.158755794_158755798del	GRCh37
NC_000005.8:g.158688372_158688376del	NCBI36
NG_009618.1:g.6685_6689del , LRG_71:g.6685_6689del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1643_-149+1647del	ENSP00000512849.1:n.-149+1643_-149+1647del
ENST00000696751.1:c.-1+1643_-1+1647del	ENSP00000512850.1:n.-1+1643_-1+1647del
ENST00000696752.1:n.432+1643_432+1647del
ENST00000231228.3:c.-1+1643_-1+1647del MANE Select	ENSP00000231228.2:n.-1+1643_-1+1647del
ENST00000231228.2:c.-1+1643_-1+1647del	ENSP00000231228.2:n.-1+1643_-1+1647del
NM_002187.2:c.-1+1643_-1+1647del , LRG_71t1:c.-1+1643_-1+1647del	NP_002178.2:n.-1+1643_-1+1647del
NM_002187.3:c.-1+1643_-1+1647del MANE Select	NP_002178.2:n.-1+1643_-1+1647del