Canonical Allele Identifier: CA447510889
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1380578064
gnomAD v3: 5-159320364-A-G
gnomAD v4: 5-159320364-A-G
MyVariant Identifiers: chr5:g.158747372A>G (hg19) chr5:g.159320364A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320364A>G , CM000667.2:g.159320364A>G GRCh38
NC_000005.9:g.158747372A>G , CM000667.1:g.158747372A>G GRCh37
NC_000005.8:g.158679950A>G NCBI36
NG_009618.1:g.15110T>C , LRG_71:g.15110T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.9T>C ENSP00000512849.1:p.Asp3=
ENST00000696751.1:c.*134T>C ENSP00000512850.1:n.*134T>C
ENST00000231228.3:c.639T>C MANE Select ENSP00000231228.2:p.Asp213=
ENST00000231228.2:c.639T>C ENSP00000231228.2:p.Asp213=
NM_002187.2:c.639T>C , LRG_71t1:c.639T>C NP_002178.2:p.Asp213=
NM_002187.3:c.639T>C MANE Select NP_002178.2:p.Asp213=
Search 100 bp 5'
Search 100 bp 3'