Canonical Allele Identifier: CA2578471157

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322996_159323002del , CM000667.2:g.159322996_159323002del	GRCh38
NC_000005.9:g.158750004_158750010del , CM000667.1:g.158750004_158750010del	GRCh37
NC_000005.8:g.158682582_158682588del	NCBI36
NG_009618.1:g.12472_12478del , LRG_71:g.12472_12478del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2482_-148-2476del	ENSP00000512849.1:n.-148-2482_-148-2476del
ENST00000696751.1:c.364+52_364+58del	ENSP00000512850.1:n.364+52_364+58del
ENST00000231228.3:c.364+52_364+58del MANE Select	ENSP00000231228.2:n.364+52_364+58del
ENST00000231228.2:c.364+52_364+58del	ENSP00000231228.2:n.364+52_364+58del
NM_002187.2:c.364+52_364+58del , LRG_71t1:c.364+52_364+58del	NP_002178.2:n.364+52_364+58del
XR_001742945.1:n.147+2400_147+2406del
NM_002187.3:c.364+52_364+58del MANE Select	NP_002178.2:n.364+52_364+58del