Canonical Allele Identifier: CA2769108405
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315947A>G , CM000667.2:g.159315947A>G GRCh38
NC_000005.9:g.158742955A>G , CM000667.1:g.158742955A>G GRCh37
NC_000005.8:g.158675533A>G NCBI36
NG_009618.1:g.19527T>C , LRG_71:g.19527T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*154T>C ENSP00000512849.1:n.*154T>C
ENST00000696751.1:c.*636T>C ENSP00000512850.1:n.*636T>C
ENST00000231228.3:c.*154T>C MANE Select ENSP00000231228.2:n.*154T>C
ENST00000231228.2:c.*154T>C ENSP00000231228.2:n.*154T>C
NM_002187.2:c.*154T>C , LRG_71t1:c.*154T>C NP_002178.2:n.*154T>C
NM_002187.3:c.*154T>C MANE Select NP_002178.2:n.*154T>C
Search 100 bp 5'
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