Canonical Allele Identifier: CA2676264670

Gene: IL12B

Linked Data

• gnomAD v4: 5-159316210-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316210C>G , CM000667.2:g.159316210C>G	GRCh38
NC_000005.9:g.158743218C>G , CM000667.1:g.158743218C>G	GRCh37
NC_000005.8:g.158675796C>G	NCBI36
NG_009618.1:g.19264G>C , LRG_71:g.19264G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*1-110G>C	ENSP00000512849.1:n.*1-110G>C
ENST00000696751.1:c.*483-110G>C	ENSP00000512850.1:n.*483-110G>C
ENST00000231228.3:c.*1-110G>C MANE Select	ENSP00000231228.2:n.*1-110G>C
ENST00000231228.2:c.*1-110G>C	ENSP00000231228.2:n.*1-110G>C
NM_002187.2:c.*1-110G>C , LRG_71t1:c.*1-110G>C	NP_002178.2:n.*1-110G>C
NM_002187.3:c.*1-110G>C MANE Select	NP_002178.2:n.*1-110G>C