Canonical Allele Identifier: CA1595018285

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322629_159322636delinsTTGGGTAG , CM000667.2:g.159322629_159322636delinsTTGGGTAG	GRCh38
NC_000005.9:g.158749637_158749644delinsTTGGGTAG , CM000667.1:g.158749637_158749644delinsTTGGGTAG	GRCh37
NC_000005.8:g.158682215_158682222delinsTTGGGTAG	NCBI36
NG_009618.1:g.12838_12845delinsCTACCCAA , LRG_71:g.12838_12845delinsCTACCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2116_-148-2109delinsCTACCCAA	ENSP00000512849.1:n.-148-2116_-148-2109delinsCTACCCAA
ENST00000696751.1:c.364+418_364+425delinsCTACCCAA	ENSP00000512850.1:n.364+418_364+425delinsCTACCCAA
ENST00000231228.3:c.365-125_365-118delinsCTACCCAA MANE Select	ENSP00000231228.2:n.365-125_365-118delinsCTACCCAA
ENST00000231228.2:c.365-125_365-118delinsCTACCCAA	ENSP00000231228.2:n.365-125_365-118delinsCTACCCAA
NM_002187.2:c.365-125_365-118delinsCTACCCAA , LRG_71t1:c.365-125_365-118delinsCTACCCAA	NP_002178.2:n.365-125_365-118delinsCTACCCAA
XR_001742945.1:n.147+2033_147+2040delinsTTGGGTAG
NM_002187.3:c.365-125_365-118delinsCTACCCAA MANE Select	NP_002178.2:n.365-125_365-118delinsCTACCCAA