Canonical Allele Identifier: CA129826454
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs953392633
gnomAD v3: 5-159319999-A-T
gnomAD v4: 5-159319999-A-T
MyVariant Identifiers: chr5:g.158747007A>T (hg19) chr5:g.159319999A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159319999A>T , CM000667.2:g.159319999A>T GRCh38
NC_000005.9:g.158747007A>T , CM000667.1:g.158747007A>T GRCh37
NC_000005.8:g.158679585A>T NCBI36
NG_009618.1:g.15475T>A , LRG_71:g.15475T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+307T>A ENSP00000512849.1:n.67+307T>A
ENST00000696751.1:c.*192+307T>A ENSP00000512850.1:n.*192+307T>A
ENST00000231228.3:c.697+307T>A MANE Select ENSP00000231228.2:n.697+307T>A
ENST00000231228.2:c.697+307T>A ENSP00000231228.2:n.697+307T>A
NM_002187.2:c.697+307T>A , LRG_71t1:c.697+307T>A NP_002178.2:n.697+307T>A
NM_002187.3:c.697+307T>A MANE Select NP_002178.2:n.697+307T>A
Search 100 bp 5'
Search 100 bp 3'