Canonical Allele Identifier: CA150362862
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1039595294
gnomAD v3: 6-155427875-T-C
gnomAD v4: 6-155427875-T-C
MyVariant Identifiers: chr6:g.155749009T>C (hg19) chr6:g.155427875T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427875T>C , CM000668.2:g.155427875T>C GRCh38
NC_000006.11:g.155749009T>C , CM000668.1:g.155749009T>C GRCh37
NC_000006.10:g.155790701T>C NCBI36
NG_011995.1:g.33029A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+919A>G MANE Select ENSP00000159060.2:n.1145+919A>G
ENST00000159060.2:c.1145+919A>G ENSP00000159060.2:n.1145+919A>G
NM_015718.2:c.1145+919A>G NP_056533.1:n.1145+919A>G
NM_015718.3:c.1145+919A>G MANE Select NP_056533.1:n.1145+919A>G
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