Canonical Allele Identifier: CA3538760
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs763525702
ExAC: 5:158747413 G / C
gnomAD v2: 5-158747413-G-C
MyVariant Identifiers: chr5:g.158747413G>C (hg19) chr5:g.159320405G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320405G>C , CM000667.2:g.159320405G>C GRCh38
NC_000005.9:g.158747413G>C , CM000667.1:g.158747413G>C GRCh37
NC_000005.8:g.158679991G>C NCBI36
NG_009618.1:g.15069C>G , LRG_71:g.15069C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-33C>G ENSP00000512849.1:n.-33C>G
ENST00000696751.1:c.*93C>G ENSP00000512850.1:n.*93C>G
ENST00000231228.3:c.598C>G MANE Select ENSP00000231228.2:p.Pro200Ala
ENST00000231228.2:c.598C>G ENSP00000231228.2:p.Pro200Ala
NM_002187.2:c.598C>G , LRG_71t1:c.598C>G NP_002178.2:p.Pro200Ala
NM_002187.3:c.598C>G MANE Select NP_002178.2:p.Pro200Ala
Search 100 bp 5'
Search 100 bp 3'