Canonical Allele Identifier: CA2710493739
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs2113025419
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159319991G>C , CM000667.2:g.159319991G>C GRCh38
NC_000005.9:g.158746999G>C , CM000667.1:g.158746999G>C GRCh37
NC_000005.8:g.158679577G>C NCBI36
NG_009618.1:g.15483C>G , LRG_71:g.15483C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.67+315C>G ENSP00000512849.1:n.67+315C>G
ENST00000696751.1:c.*192+315C>G ENSP00000512850.1:n.*192+315C>G
ENST00000231228.3:c.697+315C>G MANE Select ENSP00000231228.2:n.697+315C>G
ENST00000231228.2:c.697+315C>G ENSP00000231228.2:n.697+315C>G
NM_002187.2:c.697+315C>G , LRG_71t1:c.697+315C>G NP_002178.2:n.697+315C>G
NM_002187.3:c.697+315C>G MANE Select NP_002178.2:n.697+315C>G
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