Canonical Allele Identifier: CA2173940651
Gene: DUOX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45103860A= , CM000677.2:g.45103860A= GRCh38
NC_000015.9:g.45396058A= , CM000677.1:g.45396058A= GRCh37
NC_000015.8:g.43183350A= NCBI36
NG_009447.1:g.15302T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389039.11:c.2654+100T= MANE Select ENSP00000373691.7:n.2654+100T=
ENST00000389039.10:c.2654+100T= ENSP00000373691.6:n.2654+100T=
ENST00000558383.1:n.4385+100T=
ENST00000603300.1:c.2654+100T= ENSP00000475084.1:n.2654+100T=
NM_014080.4:c.2654+100T= NP_054799.4:n.2654+100T=
XM_005254421.2:c.2654+100T= XP_005254478.1:n.2654+100T=
NM_001363711.1:c.2654+100T= NP_001350640.1:n.2654+100T=
NM_001363711.2:c.2654+100T= MANE Select NP_001350640.1:n.2654+100T=
NM_014080.5:c.2654+100T= NP_054799.4:n.2654+100T=