Canonical Allele Identifier: CA392268528
Gene: DUOX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45396170A>C (hg19) chr15:g.45103972A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45103972A>C , CM000677.2:g.45103972A>C GRCh38
NC_000015.9:g.45396170A>C , CM000677.1:g.45396170A>C GRCh37
NC_000015.8:g.43183462A>C NCBI36
NG_009447.1:g.15190T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.2642T>G MANE Select ENSP00000373691.7:p.Phe881Cys
ENST00000389039.10:c.2642T>G ENSP00000373691.6:p.Phe881Cys
ENST00000558383.1:n.4373T>G
ENST00000603300.1:c.2642T>G ENSP00000475084.1:p.Phe881Cys
NM_014080.4:c.2642T>G NP_054799.4:p.Phe881Cys
XM_005254421.2:c.2642T>G XP_005254478.1:p.Phe881Cys
NM_001363711.1:c.2642T>G NP_001350640.1:p.Phe881Cys
NM_001363711.2:c.2642T>G MANE Select NP_001350640.1:p.Phe881Cys
NM_014080.5:c.2642T>G NP_054799.4:p.Phe881Cys
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