Canonical Allele Identifier: CA1674710955
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1776777121
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427845T>C , CM000668.2:g.155427845T>C GRCh38
NC_000006.11:g.155748979T>C , CM000668.1:g.155748979T>C GRCh37
NC_000006.10:g.155790671T>C NCBI36
NG_011995.1:g.33059A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+949A>G MANE Select ENSP00000159060.2:n.1145+949A>G
ENST00000159060.2:c.1145+949A>G ENSP00000159060.2:n.1145+949A>G
NM_015718.2:c.1145+949A>G NP_056533.1:n.1145+949A>G
NM_015718.3:c.1145+949A>G MANE Select NP_056533.1:n.1145+949A>G
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