Canonical Allele Identifier: CA1674710951

Gene: NOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155427835A= , CM000668.2:g.155427835A=	GRCh38
NC_000006.11:g.155748969A= , CM000668.1:g.155748969A=	GRCh37
NC_000006.10:g.155790661A=	NCBI36
NG_011995.1:g.33069T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000159060.3:c.1145+959T= MANE Select	ENSP00000159060.2:n.1145+959T=
ENST00000159060.2:c.1145+959T=	ENSP00000159060.2:n.1145+959T=
NM_015718.2:c.1145+959T=	NP_056533.1:n.1145+959T=
NM_015718.3:c.1145+959T= MANE Select	NP_056533.1:n.1145+959T=