Canonical Allele Identifier: CA1778232048
Gene: IDO2 HGNC NCBI

Linked Data

dbSNP Id: rs2160860
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.39965626A>C , CM000670.2:g.39965626A>C GRCh38
NC_000008.10:g.39823145A>C , CM000670.1:g.39823145A>C GRCh37
NC_000008.9:g.39942302A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502986.4:c.195+1923A>C MANE Select ENSP00000443432.2:n.195+1923A>C
ENST00000502986.3:c.195+1923A>C ENSP00000443432.2:n.195+1923A>C
ENST00000343295.8:n.817+1923A>C
ENST00000389060.8:c.195+1923A>C ENSP00000426447.1:n.195+1923A>C
ENST00000502986.2:c.234+1923A>C ENSP00000443432.1:n.234+1923A>C
NM_194294.2:c.234+1923A>C NP_919270.2:n.234+1923A>C
NM_194294.3:c.234+1923A>C NP_919270.2:n.234+1923A>C
NM_001395206.1:c.195+1923A>C NP_001382135.1:n.195+1923A>C
NM_194294.5:c.195+1923A>C MANE Select NP_919270.3:n.195+1923A>C
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