Canonical Allele Identifier: CA2773665301
Gene: NOX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427874C>A , CM000668.2:g.155427874C>A GRCh38
NC_000006.11:g.155749008C>A , CM000668.1:g.155749008C>A GRCh37
NC_000006.10:g.155790700C>A NCBI36
NG_011995.1:g.33030G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+920G>T MANE Select ENSP00000159060.2:n.1145+920G>T
ENST00000159060.2:c.1145+920G>T ENSP00000159060.2:n.1145+920G>T
NM_015718.2:c.1145+920G>T NP_056533.1:n.1145+920G>T
NM_015718.3:c.1145+920G>T MANE Select NP_056533.1:n.1145+920G>T
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