Canonical Allele Identifier: CA2173940655
Gene: DUOX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45103866A= , CM000677.2:g.45103866A= GRCh38
NC_000015.9:g.45396064A= , CM000677.1:g.45396064A= GRCh37
NC_000015.8:g.43183356A= NCBI36
NG_009447.1:g.15296T=

Transcript Alleles

HGVS Amino-acid change
ENST00000389039.11:c.2654+94T= MANE Select ENSP00000373691.7:n.2654+94T=
ENST00000389039.10:c.2654+94T= ENSP00000373691.6:n.2654+94T=
ENST00000558383.1:n.4385+94T=
ENST00000603300.1:c.2654+94T= ENSP00000475084.1:n.2654+94T=
NM_014080.4:c.2654+94T= NP_054799.4:n.2654+94T=
XM_005254421.2:c.2654+94T= XP_005254478.1:n.2654+94T=
NM_001363711.1:c.2654+94T= NP_001350640.1:n.2654+94T=
NM_001363711.2:c.2654+94T= MANE Select NP_001350640.1:n.2654+94T=
NM_014080.5:c.2654+94T= NP_054799.4:n.2654+94T=
Search 100 bp 5'
Search 100 bp 3'