Canonical Allele Identifier: CA3538755
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 1040966
ClinVar RCV Id: RCV001344704
dbSNP Id: rs138127918
ExAC: 5:158747388 A / G
gnomAD v2: 5-158747388-A-G
gnomAD v3: 5-159320380-A-G
gnomAD v4: 5-159320380-A-G
MyVariant Identifiers: chr5:g.158747388A>G (hg19) chr5:g.159320380A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320380A>G , CM000667.2:g.159320380A>G GRCh38
NC_000005.9:g.158747388A>G , CM000667.1:g.158747388A>G GRCh37
NC_000005.8:g.158679966A>G NCBI36
NG_009618.1:g.15094T>C , LRG_71:g.15094T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-8T>C ENSP00000512849.1:n.-8T>C
ENST00000696751.1:c.*118T>C ENSP00000512850.1:n.*118T>C
ENST00000231228.3:c.623T>C MANE Select ENSP00000231228.2:p.Ile208Thr
ENST00000231228.2:c.623T>C ENSP00000231228.2:p.Ile208Thr
NM_002187.2:c.623T>C , LRG_71t1:c.623T>C NP_002178.2:p.Ile208Thr
NM_002187.3:c.623T>C MANE Select NP_002178.2:p.Ile208Thr
Search 100 bp 5'
Search 100 bp 3'