Canonical Allele Identifier: CA1778252338
Gene: IDO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.40005286C= , CM000670.2:g.40005286C= GRCh38
NC_000008.10:g.39862805C= , CM000670.1:g.39862805C= GRCh37
NC_000008.9:g.39981962C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502986.4:c.668-41C= MANE Select ENSP00000443432.2:n.668-41C=
ENST00000502986.3:c.668-41C= ENSP00000443432.2:n.668-41C=
ENST00000343295.8:n.2971-8279C=
ENST00000389060.8:c.668-41C= ENSP00000426447.1:n.668-41C=
ENST00000418094.1:n.347-8279C=
ENST00000502986.2:c.707-41C= ENSP00000443432.1:n.707-41C=
NM_194294.2:c.707-41C= NP_919270.2:n.707-41C=
NM_194294.3:c.707-41C= NP_919270.2:n.707-41C=
NM_001395206.1:c.668-41C= NP_001382135.1:n.668-41C=
NM_194294.5:c.668-41C= MANE Select NP_919270.3:n.668-41C=