Canonical Allele Identifier: CA3538862
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs778518679
ExAC: 5:158750197 T / C
gnomAD v2: 5-158750197-T-C
gnomAD v4: 5-159323189-T-C
MyVariant Identifiers: chr5:g.158750197T>C (hg19) chr5:g.159323189T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323189T>C , CM000667.2:g.159323189T>C GRCh38
NC_000005.9:g.158750197T>C , CM000667.1:g.158750197T>C GRCh37
NC_000005.8:g.158682775T>C NCBI36
NG_009618.1:g.12285A>G , LRG_71:g.12285A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2669A>G ENSP00000512849.1:n.-148-2669A>G
ENST00000696751.1:c.229A>G ENSP00000512850.1:p.Ile77Val
ENST00000231228.3:c.229A>G MANE Select ENSP00000231228.2:p.Ile77Val
ENST00000231228.2:c.229A>G ENSP00000231228.2:p.Ile77Val
NM_002187.2:c.229A>G , LRG_71t1:c.229A>G NP_002178.2:p.Ile77Val
XR_001742945.1:n.148-2345T>C
NM_002187.3:c.229A>G MANE Select NP_002178.2:p.Ile77Val
Search 100 bp 5'
Search 100 bp 3'