Canonical Allele Identifier: CA2579151013
Gene: IDO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.40005287T>C , CM000670.2:g.40005287T>C GRCh38
NC_000008.10:g.39862806T>C , CM000670.1:g.39862806T>C GRCh37
NC_000008.9:g.39981963T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502986.4:c.668-40T>C MANE Select ENSP00000443432.2:n.668-40T>C
ENST00000502986.3:c.668-40T>C ENSP00000443432.2:n.668-40T>C
ENST00000343295.8:n.2971-8278T>C
ENST00000389060.8:c.668-40T>C ENSP00000426447.1:n.668-40T>C
ENST00000418094.1:n.347-8278T>C
ENST00000502986.2:c.707-40T>C ENSP00000443432.1:n.707-40T>C
NM_194294.2:c.707-40T>C NP_919270.2:n.707-40T>C
NM_194294.3:c.707-40T>C NP_919270.2:n.707-40T>C
NM_001395206.1:c.668-40T>C NP_001382135.1:n.668-40T>C
NM_194294.5:c.668-40T>C MANE Select NP_919270.3:n.668-40T>C