Canonical Allele Identifier: CA371045582

Gene: IDO2

Linked Data

• dbSNP Id: rs1563441605
• gnomAD v4: 8-40005368-T-C
• MyVariant Identifiers: chr8:g.39862887T>C (hg19) ; chr8:g.40005368T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.40005368T>C , CM000670.2:g.40005368T>C	GRCh38
NC_000008.10:g.39862887T>C , CM000670.1:g.39862887T>C	GRCh37
NC_000008.9:g.39982044T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502986.4:c.709T>C MANE Select	ENSP00000443432.2:p.Phe237Leu
ENST00000502986.3:c.709T>C	ENSP00000443432.2:p.Phe237Leu
ENST00000343295.8:n.2971-8197T>C
ENST00000389060.8:c.709T>C	ENSP00000426447.1:p.Phe237Leu
ENST00000418094.1:n.347-8197T>C
ENST00000502986.2:c.748T>C	ENSP00000443432.1:p.Phe250Leu
NM_194294.2:c.748T>C	NP_919270.2:p.Phe250Leu
NM_194294.3:c.748T>C	NP_919270.2:p.Phe250Leu
NM_001395206.1:c.709T>C	NP_001382135.1:p.Phe237Leu
NM_194294.5:c.709T>C MANE Select	NP_919270.3:p.Phe237Leu