Canonical Allele Identifier: CA3538891
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs772150335
ExAC: 5:158750389 G / T
gnomAD v2: 5-158750389-G-T
gnomAD v4: 5-159323381-G-T
MyVariant Identifiers: chr5:g.158750389G>T (hg19) chr5:g.159323381G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323381G>T , CM000667.2:g.159323381G>T GRCh38
NC_000005.9:g.158750389G>T , CM000667.1:g.158750389G>T GRCh37
NC_000005.8:g.158682967G>T NCBI36
NG_009618.1:g.12093C>A , LRG_71:g.12093C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2861C>A ENSP00000512849.1:n.-148-2861C>A
ENST00000696751.1:c.89-52C>A ENSP00000512850.1:n.89-52C>A
ENST00000231228.3:c.89-52C>A MANE Select ENSP00000231228.2:n.89-52C>A
ENST00000231228.2:c.89-52C>A ENSP00000231228.2:n.89-52C>A
NM_002187.2:c.89-52C>A , LRG_71t1:c.89-52C>A NP_002178.2:n.89-52C>A
XR_001742945.1:n.148-2153G>T
NM_002187.3:c.89-52C>A MANE Select NP_002178.2:n.89-52C>A
Search 100 bp 5'
Search 100 bp 3'