Canonical Allele Identifier: CA2769108044

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320010_159320011insTG , CM000667.2:g.159320010_159320011insTG	GRCh38
NC_000005.9:g.158747018_158747019insTG , CM000667.1:g.158747018_158747019insTG	GRCh37
NC_000005.8:g.158679596_158679597insTG	NCBI36
NG_009618.1:g.15463_15464insCA , LRG_71:g.15463_15464insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.67+295_67+296insCA	ENSP00000512849.1:n.67+295_67+296insCA
ENST00000696751.1:c.*192+295_*192+296insCA	ENSP00000512850.1:n.*192+295_*192+296insCA
ENST00000231228.3:c.697+295_697+296insCA MANE Select	ENSP00000231228.2:n.697+295_697+296insCA
ENST00000231228.2:c.697+295_697+296insCA	ENSP00000231228.2:n.697+295_697+296insCA
NM_002187.2:c.697+295_697+296insCA , LRG_71t1:c.697+295_697+296insCA	NP_002178.2:n.697+295_697+296insCA
NM_002187.3:c.697+295_697+296insCA MANE Select	NP_002178.2:n.697+295_697+296insCA