Canonical Allele Identifier: CA3538890
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs368447540
ExAC: 5:158750385 C / T
gnomAD v2: 5-158750385-C-T
gnomAD v3: 5-159323377-C-T
gnomAD v4: 5-159323377-C-T
MyVariant Identifiers: chr5:g.158750385C>T (hg19) chr5:g.159323377C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323377C>T , CM000667.2:g.159323377C>T GRCh38
NC_000005.9:g.158750385C>T , CM000667.1:g.158750385C>T GRCh37
NC_000005.8:g.158682963C>T NCBI36
NG_009618.1:g.12097G>A , LRG_71:g.12097G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2857G>A ENSP00000512849.1:n.-148-2857G>A
ENST00000696751.1:c.89-48G>A ENSP00000512850.1:n.89-48G>A
ENST00000231228.3:c.89-48G>A MANE Select ENSP00000231228.2:n.89-48G>A
ENST00000231228.2:c.89-48G>A ENSP00000231228.2:n.89-48G>A
NM_002187.2:c.89-48G>A , LRG_71t1:c.89-48G>A NP_002178.2:n.89-48G>A
XR_001742945.1:n.148-2157C>T
NM_002187.3:c.89-48G>A MANE Select NP_002178.2:n.89-48G>A
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