Canonical Allele Identifier: CA571189690
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1387461799
gnomAD v2: 6-155749003-C-T
gnomAD v3: 6-155427869-C-T
gnomAD v4: 6-155427869-C-T
MyVariant Identifiers: chr6:g.155749003C>T (hg19) chr6:g.155427869C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427869C>T , CM000668.2:g.155427869C>T GRCh38
NC_000006.11:g.155749003C>T , CM000668.1:g.155749003C>T GRCh37
NC_000006.10:g.155790695C>T NCBI36
NG_011995.1:g.33035G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+925G>A MANE Select ENSP00000159060.2:n.1145+925G>A
ENST00000159060.2:c.1145+925G>A ENSP00000159060.2:n.1145+925G>A
NM_015718.2:c.1145+925G>A NP_056533.1:n.1145+925G>A
NM_015718.3:c.1145+925G>A MANE Select NP_056533.1:n.1145+925G>A
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