Canonical Allele Identifier: CA1595020875

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328898_159328899delinsTG , CM000667.2:g.159328898_159328899delinsTG	GRCh38
NC_000005.9:g.158755906_158755907delinsTG , CM000667.1:g.158755906_158755907delinsTG	GRCh37
NC_000005.8:g.158688484_158688485delinsTG	NCBI36
NG_009618.1:g.6575_6576delinsCA , LRG_71:g.6575_6576delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+1533_-149+1534delinsCA	ENSP00000512849.1:n.-149+1533_-149+1534de...
ENST00000696751.1:c.-1+1533_-1+1534delinsCA	ENSP00000512850.1:n.-1+1533_-1+1534delins...
ENST00000696752.1:n.432+1533_432+1534delinsCA
ENST00000231228.3:c.-1+1533_-1+1534delinsCA MANE Select	ENSP00000231228.2:n.-1+1533_-1+1534delins...
ENST00000231228.2:c.-1+1533_-1+1534delinsCA	ENSP00000231228.2:n.-1+1533_-1+1534delins...
NM_002187.2:c.-1+1533_-1+1534delinsCA , LRG_71t1:c.-1+1533_-1+1534delinsCA	NP_002178.2:n.-1+1533_-1+1534delinsCA
NM_002187.3:c.-1+1533_-1+1534delinsCA MANE Select	NP_002178.2:n.-1+1533_-1+1534delinsCA