Canonical Allele Identifier: CA175887281
Gene: IDO2 HGNC NCBI

Linked Data

dbSNP Id: rs778054053
gnomAD v4: 8-40005275-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.40005275C>T , CM000670.2:g.40005275C>T GRCh38
NC_000008.10:g.39862794C>T , CM000670.1:g.39862794C>T GRCh37
NC_000008.9:g.39981951C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502986.4:c.668-52C>T MANE Select ENSP00000443432.2:n.668-52C>T
ENST00000502986.3:c.668-52C>T ENSP00000443432.2:n.668-52C>T
ENST00000343295.8:n.2971-8290C>T
ENST00000389060.8:c.668-52C>T ENSP00000426447.1:n.668-52C>T
ENST00000418094.1:n.347-8290C>T
ENST00000502986.2:c.707-52C>T ENSP00000443432.1:n.707-52C>T
NM_194294.2:c.707-52C>T NP_919270.2:n.707-52C>T
NM_194294.3:c.707-52C>T NP_919270.2:n.707-52C>T
NM_001395206.1:c.668-52C>T NP_001382135.1:n.668-52C>T
NM_194294.5:c.668-52C>T MANE Select NP_919270.3:n.668-52C>T