Canonical Allele Identifier: CA3538758
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs776207541
ExAC: 5:158747402 C / T
gnomAD v2: 5-158747402-C-T
gnomAD v4: 5-159320394-C-T
MyVariant Identifiers: chr5:g.158747402C>T (hg19) chr5:g.159320394C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320394C>T , CM000667.2:g.159320394C>T GRCh38
NC_000005.9:g.158747402C>T , CM000667.1:g.158747402C>T GRCh37
NC_000005.8:g.158679980C>T NCBI36
NG_009618.1:g.15080G>A , LRG_71:g.15080G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-22G>A ENSP00000512849.1:n.-22G>A
ENST00000696751.1:c.*104G>A ENSP00000512850.1:n.*104G>A
ENST00000231228.3:c.609G>A MANE Select ENSP00000231228.2:p.Glu203=
ENST00000231228.2:c.609G>A ENSP00000231228.2:p.Glu203=
NM_002187.2:c.609G>A , LRG_71t1:c.609G>A NP_002178.2:p.Glu203=
NM_002187.3:c.609G>A MANE Select NP_002178.2:p.Glu203=
Search 100 bp 5'
Search 100 bp 3'