Canonical Allele Identifier: CA1595045656
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1753981626
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315909A>G , CM000667.2:g.159315909A>G GRCh38
NC_000005.9:g.158742917A>G , CM000667.1:g.158742917A>G GRCh37
NC_000005.8:g.158675495A>G NCBI36
NG_009618.1:g.19565T>C , LRG_71:g.19565T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*192T>C ENSP00000512849.1:n.*192T>C
ENST00000696751.1:c.*674T>C ENSP00000512850.1:n.*674T>C
ENST00000231228.3:c.*192T>C MANE Select ENSP00000231228.2:n.*192T>C
ENST00000231228.2:c.*192T>C ENSP00000231228.2:n.*192T>C
NM_002187.2:c.*192T>C , LRG_71t1:c.*192T>C NP_002178.2:n.*192T>C
NM_002187.3:c.*192T>C MANE Select NP_002178.2:n.*192T>C
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