Canonical Allele Identifier: CA129823351
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs908580982
gnomAD v2: 5-158743198-G-A
gnomAD v3: 5-159316190-G-A
gnomAD v4: 5-159316190-G-A
MyVariant Identifiers: chr5:g.158743198G>A (hg19) chr5:g.159316190G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316190G>A , CM000667.2:g.159316190G>A GRCh38
NC_000005.9:g.158743198G>A , CM000667.1:g.158743198G>A GRCh37
NC_000005.8:g.158675776G>A NCBI36
NG_009618.1:g.19284C>T , LRG_71:g.19284C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*1-90C>T ENSP00000512849.1:n.*1-90C>T
ENST00000696751.1:c.*483-90C>T ENSP00000512850.1:n.*483-90C>T
ENST00000231228.3:c.*1-90C>T MANE Select ENSP00000231228.2:n.*1-90C>T
ENST00000231228.2:c.*1-90C>T ENSP00000231228.2:n.*1-90C>T
NM_002187.2:c.*1-90C>T , LRG_71t1:c.*1-90C>T NP_002178.2:n.*1-90C>T
NM_002187.3:c.*1-90C>T MANE Select NP_002178.2:n.*1-90C>T
Search 100 bp 5'
Search 100 bp 3'