Canonical Allele Identifier: CA2710492184
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs2113030795
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323438A>C , CM000667.2:g.159323438A>C GRCh38
NC_000005.9:g.158750446A>C , CM000667.1:g.158750446A>C GRCh37
NC_000005.8:g.158683024A>C NCBI36
NG_009618.1:g.12036T>G , LRG_71:g.12036T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2918T>G ENSP00000512849.1:n.-148-2918T>G
ENST00000696751.1:c.89-109T>G ENSP00000512850.1:n.89-109T>G
ENST00000231228.3:c.89-109T>G MANE Select ENSP00000231228.2:n.89-109T>G
ENST00000231228.2:c.89-109T>G ENSP00000231228.2:n.89-109T>G
NM_002187.2:c.89-109T>G , LRG_71t1:c.89-109T>G NP_002178.2:n.89-109T>G
XR_001742945.1:n.148-2096A>C
NM_002187.3:c.89-109T>G MANE Select NP_002178.2:n.89-109T>G
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