Canonical Allele Identifier: CA150362877
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs534600110
gnomAD v3: 6-155427888-TTCCTCCTCC-T
gnomAD v4: 6-155427888-TTCCTCCTCC-T
MyVariant Identifiers: chr6:g.155749023_155749031del (hg19) chr6:g.155427889_155427897del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427899_155427907del , CM000668.2:g.155427899_155427907del GRCh38
NC_000006.11:g.155749033_155749041del , CM000668.1:g.155749033_155749041del GRCh37
NC_000006.10:g.155790725_155790733del NCBI36
NG_011995.1:g.33007_33015del

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+897_1145+905del MANE Select ENSP00000159060.2:n.1145+897_1145+905del
ENST00000159060.2:c.1145+897_1145+905del ENSP00000159060.2:n.1145+897_1145+905del
NM_015718.2:c.1145+897_1145+905del NP_056533.1:n.1145+897_1145+905del
NM_015718.3:c.1145+897_1145+905del MANE Select NP_056533.1:n.1145+897_1145+905del
Search 100 bp 5'
Search 100 bp 3'