Canonical Allele Identifier: CA821173863
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1459299204
gnomAD v3: 6-155427878-T-C
gnomAD v4: 6-155427878-T-C
MyVariant Identifiers: chr6:g.155749012T>C (hg19) chr6:g.155427878T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427878T>C , CM000668.2:g.155427878T>C GRCh38
NC_000006.11:g.155749012T>C , CM000668.1:g.155749012T>C GRCh37
NC_000006.10:g.155790704T>C NCBI36
NG_011995.1:g.33026A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+916A>G MANE Select ENSP00000159060.2:n.1145+916A>G
ENST00000159060.2:c.1145+916A>G ENSP00000159060.2:n.1145+916A>G
NM_015718.2:c.1145+916A>G NP_056533.1:n.1145+916A>G
NM_015718.3:c.1145+916A>G MANE Select NP_056533.1:n.1145+916A>G
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