Canonical Allele Identifier: CA12423571
Gene: NOX3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs231950

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155428027G>A , CM000668.2:g.155428027G>A GRCh38
NC_000006.10:g.155790853G>A NCBI36
NC_000006.11:g.155749161G>A , CM000668.1:g.155749161G>A GRCh37
NG_011995.1:g.32877C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000159060.2:c.1145+767C>T ENSP00000159060.2:p.=
NM_015718.2:c.1145+767C>T VV NP_056533.1:p.=