Canonical Allele Identifier: CA4725237
Gene: IDO2 HGNC NCBI

Linked Data

dbSNP Id: rs770513202
gnomAD v2: 8-39862797-A-G
gnomAD v3: 8-40005278-A-G
gnomAD v4: 8-40005278-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.40005278A>G , CM000670.2:g.40005278A>G GRCh38
NC_000008.10:g.39862797A>G , CM000670.1:g.39862797A>G GRCh37
NC_000008.9:g.39981954A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502986.4:c.668-49A>G MANE Select ENSP00000443432.2:n.668-49A>G
ENST00000502986.3:c.668-49A>G ENSP00000443432.2:n.668-49A>G
ENST00000343295.8:n.2971-8287A>G
ENST00000389060.8:c.668-49A>G ENSP00000426447.1:n.668-49A>G
ENST00000418094.1:n.347-8287A>G
ENST00000502986.2:c.707-49A>G ENSP00000443432.1:n.707-49A>G
NM_194294.2:c.707-49A>G NP_919270.2:n.707-49A>G
NM_194294.3:c.707-49A>G NP_919270.2:n.707-49A>G
NM_001395206.1:c.668-49A>G NP_001382135.1:n.668-49A>G
NM_194294.5:c.668-49A>G MANE Select NP_919270.3:n.668-49A>G