Canonical Allele Identifier: CA392268516
Gene: DUOX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45396168T>C (hg19) chr15:g.45103970T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45103970T>C , CM000677.2:g.45103970T>C GRCh38
NC_000015.9:g.45396168T>C , CM000677.1:g.45396168T>C GRCh37
NC_000015.8:g.43183460T>C NCBI36
NG_009447.1:g.15192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.2644A>G MANE Select ENSP00000373691.7:p.Thr882Ala
ENST00000389039.10:c.2644A>G ENSP00000373691.6:p.Thr882Ala
ENST00000558383.1:n.4375A>G
ENST00000603300.1:c.2644A>G ENSP00000475084.1:p.Thr882Ala
NM_014080.4:c.2644A>G NP_054799.4:p.Thr882Ala
XM_005254421.2:c.2644A>G XP_005254478.1:p.Thr882Ala
NM_001363711.1:c.2644A>G NP_001350640.1:p.Thr882Ala
NM_001363711.2:c.2644A>G MANE Select NP_001350640.1:p.Thr882Ala
NM_014080.5:c.2644A>G NP_054799.4:p.Thr882Ala
Search 100 bp 5'
Search 100 bp 3'