Canonical Allele Identifier: CA1674710969

Gene: NOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155427875T= , CM000668.2:g.155427875T=	GRCh38
NC_000006.11:g.155749009T= , CM000668.1:g.155749009T=	GRCh37
NC_000006.10:g.155790701T=	NCBI36
NG_011995.1:g.33029A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000159060.3:c.1145+919A= MANE Select	ENSP00000159060.2:n.1145+919A=
ENST00000159060.2:c.1145+919A=	ENSP00000159060.2:n.1145+919A=
NM_015718.2:c.1145+919A=	NP_056533.1:n.1145+919A=
NM_015718.3:c.1145+919A= MANE Select	NP_056533.1:n.1145+919A=