Canonical Allele Identifier: CA1595017390
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754071442
gnomAD v4: 5-159320642-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320642C>T , CM000667.2:g.159320642C>T GRCh38
NC_000005.9:g.158747650C>T , CM000667.1:g.158747650C>T GRCh37
NC_000005.8:g.158680228C>T NCBI36
NG_009618.1:g.14832G>A , LRG_71:g.14832G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-122G>A ENSP00000512849.1:n.-148-122G>A
ENST00000696751.1:c.365-122G>A ENSP00000512850.1:n.365-122G>A
ENST00000231228.3:c.483-122G>A MANE Select ENSP00000231228.2:n.483-122G>A
ENST00000231228.2:c.483-122G>A ENSP00000231228.2:n.483-122G>A
NM_002187.2:c.483-122G>A , LRG_71t1:c.483-122G>A NP_002178.2:n.483-122G>A
XR_001742945.1:n.147+46C>T
NM_002187.3:c.483-122G>A MANE Select NP_002178.2:n.483-122G>A
Search 100 bp 5'
Search 100 bp 3'