Canonical Allele Identifier: CA1595018298

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322642_159322643delinsTA , CM000667.2:g.159322642_159322643delinsTA	GRCh38
NC_000005.9:g.158749650_158749651delinsTA , CM000667.1:g.158749650_158749651delinsTA	GRCh37
NC_000005.8:g.158682228_158682229delinsTA	NCBI36
NG_009618.1:g.12831_12832delinsTA , LRG_71:g.12831_12832delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2123_-148-2122delinsTA	ENSP00000512849.1:n.-148-2123_-148-2122delinsTA
ENST00000696751.1:c.364+411_364+412delinsTA	ENSP00000512850.1:n.364+411_364+412delinsTA
ENST00000231228.3:c.365-132_365-131delinsTA MANE Select	ENSP00000231228.2:n.365-132_365-131delinsTA
ENST00000231228.2:c.365-132_365-131delinsTA	ENSP00000231228.2:n.365-132_365-131delinsTA
NM_002187.2:c.365-132_365-131delinsTA , LRG_71t1:c.365-132_365-131delinsTA	NP_002178.2:n.365-132_365-131delinsTA
XR_001742945.1:n.147+2046_147+2047delinsTA
NM_002187.3:c.365-132_365-131delinsTA MANE Select	NP_002178.2:n.365-132_365-131delinsTA