Canonical Allele Identifier: CA2773665304
Gene: NOX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155427960G>A , CM000668.2:g.155427960G>A GRCh38
NC_000006.11:g.155749094G>A , CM000668.1:g.155749094G>A GRCh37
NC_000006.10:g.155790786G>A NCBI36
NG_011995.1:g.32944C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000159060.3:c.1145+834C>T MANE Select ENSP00000159060.2:n.1145+834C>T
ENST00000159060.2:c.1145+834C>T ENSP00000159060.2:n.1145+834C>T
NM_015718.2:c.1145+834C>T NP_056533.1:n.1145+834C>T
NM_015718.3:c.1145+834C>T MANE Select NP_056533.1:n.1145+834C>T