Canonical Allele Identifier: CA7292623
Gene: DIO2 HGNC NCBI

Linked Data

dbSNP Id: rs765667555

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80203010T>C , CM000676.2:g.80203010T>C GRCh38
NC_000014.8:g.80669353T>C , CM000676.1:g.80669353T>C GRCh37
NC_000014.7:g.79739106T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000438257.9:c.501A>G MANE Select ENSP00000405854.5:p.Ser167=
ENST00000555750.2:c.*339A>G ENSP00000450980.2:n.*339A>G
ENST00000422005.7:c.*302A>G ENSP00000411438.4:n.*302A>G
ENST00000438257.8:c.501A>G ENSP00000405854.4:p.Ser167=
ENST00000555750.1:c.609A>G ENSP00000450980.1:p.Ser203=
ENST00000555844.1:c.585A>G
ENST00000556811.5:c.477A>G
ENST00000557010.5:c.501A>G ENSP00000451419.1:p.Ser167=
ENST00000557125.1:c.125A>G ENSP00000450547.1:p.Gln42Arg
NM_000793.5:c.501A>G NP_000784.2:p.Ser167=
NM_001007023.3:c.609A>G NP_001007024.1:p.Ser203=
NM_001242502.1:c.*302A>G NP_001229431.1:n.*302A>G
NM_001242503.1:c.*302A>G NP_001229432.1:n.*302A>G
NM_013989.4:c.501A>G NP_054644.1:p.Ser167=
NM_000793.6:c.501A>G NP_000784.3:p.Ser167=
NM_001324462.2:c.501A>G NP_001311391.2:p.Ser167=
NM_001366496.1:c.501A>G NP_001353425.1:p.Ser167=
NM_013989.5:c.501A>G MANE Select NP_054644.1:p.Ser167=
NR_158990.1:n.641A>G
NR_158991.1:n.775A>G