Canonical Allele Identifier: CA1674710963
Gene: NOX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427863A= , CM000668.2:g.155427863A= GRCh38
NC_000006.11:g.155748997A= , CM000668.1:g.155748997A= GRCh37
NC_000006.10:g.155790689A= NCBI36
NG_011995.1:g.33041T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+931T= MANE Select ENSP00000159060.2:n.1145+931T=
ENST00000159060.2:c.1145+931T= ENSP00000159060.2:n.1145+931T=
NM_015718.2:c.1145+931T= NP_056533.1:n.1145+931T=
NM_015718.3:c.1145+931T= MANE Select NP_056533.1:n.1145+931T=
Search 100 bp 5'
Search 100 bp 3'