Canonical Allele Identifier: CA1674710957
Gene: NOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427847C= , CM000668.2:g.155427847C= GRCh38
NC_000006.11:g.155748981C= , CM000668.1:g.155748981C= GRCh37
NC_000006.10:g.155790673C= NCBI36
NG_011995.1:g.33057G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+947G= MANE Select ENSP00000159060.2:n.1145+947G=
ENST00000159060.2:c.1145+947G= ENSP00000159060.2:n.1145+947G=
NM_015718.2:c.1145+947G= NP_056533.1:n.1145+947G=
NM_015718.3:c.1145+947G= MANE Select NP_056533.1:n.1145+947G=