Canonical Allele Identifier: CA564023472
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1478547243
gnomAD v2: 5-158741925-A-G
gnomAD v3: 5-159314917-A-G
gnomAD v4: 5-159314917-A-G
MyVariant Identifiers: chr5:g.158741925A>G (hg19) chr5:g.159314917A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159314917A>G , CM000667.2:g.159314917A>G GRCh38
NC_000005.9:g.158741925A>G , CM000667.1:g.158741925A>G GRCh37
NC_000005.8:g.158674503A>G NCBI36
NG_009618.1:g.20557T>C , LRG_71:g.20557T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1184T>C ENSP00000512849.1:n.*1184T>C
ENST00000696751.1:c.*1666T>C ENSP00000512850.1:n.*1666T>C
ENST00000231228.3:c.*1184T>C MANE Select ENSP00000231228.2:n.*1184T>C
ENST00000231228.2:c.*1184T>C ENSP00000231228.2:n.*1184T>C
NM_002187.2:c.*1184T>C , LRG_71t1:c.*1184T>C NP_002178.2:n.*1184T>C
XR_941138.1:n.364-301A>G
XR_941138.2:n.431-301A>G
NM_002187.3:c.*1184T>C MANE Select NP_002178.2:n.*1184T>C
Search 100 bp 5'
Search 100 bp 3'