Canonical Allele Identifier: CA2769108170

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322302_159322307del , CM000667.2:g.159322302_159322307del	GRCh38
NC_000005.9:g.158749310_158749315del , CM000667.1:g.158749310_158749315del	GRCh37
NC_000005.8:g.158681888_158681893del	NCBI36
NG_009618.1:g.13172_13177del , LRG_71:g.13172_13177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1782_-148-1777del	ENSP00000512849.1:n.-148-1782_-148-1777del
ENST00000696751.1:c.364+752_364+757del	ENSP00000512850.1:n.364+752_364+757del
ENST00000231228.3:c.482+92_482+97del MANE Select	ENSP00000231228.2:n.482+92_482+97del
ENST00000231228.2:c.482+92_482+97del	ENSP00000231228.2:n.482+92_482+97del
NM_002187.2:c.482+92_482+97del , LRG_71t1:c.482+92_482+97del	NP_002178.2:n.482+92_482+97del
XR_001742945.1:n.147+1706_147+1711del
NM_002187.3:c.482+92_482+97del MANE Select	NP_002178.2:n.482+92_482+97del