Canonical Allele Identifier: CA1595045697

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316002_159316006delinsCAGAT , CM000667.2:g.159316002_159316006delinsCAGAT	GRCh38
NC_000005.9:g.158743010_158743014delinsCAGAT , CM000667.1:g.158743010_158743014delinsCAGAT	GRCh37
NC_000005.8:g.158675588_158675592delinsCAGAT	NCBI36
NG_009618.1:g.19468_19472delinsATCTG , LRG_71:g.19468_19472delinsATCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*95_*99delinsATCTG	ENSP00000512849.1:n.*95_*99delinsATCTG
ENST00000696751.1:c.*577_*581delinsATCTG	ENSP00000512850.1:n.*577_*581delinsATCTG
ENST00000231228.3:c.*95_*99delinsATCTG MANE Select	ENSP00000231228.2:n.*95_*99delinsATCTG
ENST00000231228.2:c.*95_*99delinsATCTG	ENSP00000231228.2:n.*95_*99delinsATCTG
NM_002187.2:c.*95_*99delinsATCTG , LRG_71t1:c.*95_*99delinsATCTG	NP_002178.2:n.*95_*99delinsATCTG
NM_002187.3:c.*95_*99delinsATCTG MANE Select	NP_002178.2:n.*95_*99delinsATCTG