Canonical Allele Identifier: CA1083508445

Gene: IL12B

Linked Data

• dbSNP Id: rs1754101926
• gnomAD v3: 5-159321991-GGC-G
• gnomAD v4: 5-159321991-GGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321992_159321993del , CM000667.2:g.159321992_159321993del	GRCh38
NC_000005.9:g.158749000_158749001del , CM000667.1:g.158749000_158749001del	GRCh37
NC_000005.8:g.158681578_158681579del	NCBI36
NG_009618.1:g.13481_13482del , LRG_71:g.13481_13482del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-1473_-148-1472del	ENSP00000512849.1:n.-148-1473_-148-1472de...
ENST00000696751.1:c.364+1061_364+1062del	ENSP00000512850.1:n.364+1061_364+1062del
ENST00000231228.3:c.482+401_482+402del MANE Select	ENSP00000231228.2:n.482+401_482+402del
ENST00000231228.2:c.482+401_482+402del	ENSP00000231228.2:n.482+401_482+402del
NM_002187.2:c.482+401_482+402del , LRG_71t1:c.482+401_482+402del	NP_002178.2:n.482+401_482+402del
XR_001742945.1:n.147+1396_147+1397del
NM_002187.3:c.482+401_482+402del MANE Select	NP_002178.2:n.482+401_482+402del