Canonical Allele Identifier: CA150362855
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1047656253
gnomAD v2: 6-155748983-T-C
gnomAD v3: 6-155427849-T-C
gnomAD v4: 6-155427849-T-C
MyVariant Identifiers: chr6:g.155748983T>C (hg19) chr6:g.155427849T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427849T>C , CM000668.2:g.155427849T>C GRCh38
NC_000006.11:g.155748983T>C , CM000668.1:g.155748983T>C GRCh37
NC_000006.10:g.155790675T>C NCBI36
NG_011995.1:g.33055A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+945A>G MANE Select ENSP00000159060.2:n.1145+945A>G
ENST00000159060.2:c.1145+945A>G ENSP00000159060.2:n.1145+945A>G
NM_015718.2:c.1145+945A>G NP_056533.1:n.1145+945A>G
NM_015718.3:c.1145+945A>G MANE Select NP_056533.1:n.1145+945A>G
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