Canonical Allele Identifier: CA1595018423

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322990_159322991delinsGT , CM000667.2:g.159322990_159322991delinsGT	GRCh38
NC_000005.9:g.158749998_158749999delinsGT , CM000667.1:g.158749998_158749999delinsGT	GRCh37
NC_000005.8:g.158682576_158682577delinsGT	NCBI36
NG_009618.1:g.12483_12484delinsAC , LRG_71:g.12483_12484delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2471_-148-2470delinsAC	ENSP00000512849.1:n.-148-2471_-148-2470delinsAC
ENST00000696751.1:c.364+63_364+64delinsAC	ENSP00000512850.1:n.364+63_364+64delinsAC
ENST00000231228.3:c.364+63_364+64delinsAC MANE Select	ENSP00000231228.2:n.364+63_364+64delinsAC
ENST00000231228.2:c.364+63_364+64delinsAC	ENSP00000231228.2:n.364+63_364+64delinsAC
NM_002187.2:c.364+63_364+64delinsAC , LRG_71t1:c.364+63_364+64delinsAC	NP_002178.2:n.364+63_364+64delinsAC
XR_001742945.1:n.147+2394_147+2395delinsGT
NM_002187.3:c.364+63_364+64delinsAC MANE Select	NP_002178.2:n.364+63_364+64delinsAC