Canonical Allele Identifier: CA821173844
Gene: NOX3 HGNC NCBI

Linked Data

dbSNP Id: rs1451967692
gnomAD v3: 6-155427860-G-A
gnomAD v4: 6-155427860-G-A
MyVariant Identifiers: chr6:g.155748994G>A (hg19) chr6:g.155427860G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427860G>A , CM000668.2:g.155427860G>A GRCh38
NC_000006.11:g.155748994G>A , CM000668.1:g.155748994G>A GRCh37
NC_000006.10:g.155790686G>A NCBI36
NG_011995.1:g.33044C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+934C>T MANE Select ENSP00000159060.2:n.1145+934C>T
ENST00000159060.2:c.1145+934C>T ENSP00000159060.2:n.1145+934C>T
NM_015718.2:c.1145+934C>T NP_056533.1:n.1145+934C>T
NM_015718.3:c.1145+934C>T MANE Select NP_056533.1:n.1145+934C>T
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