Canonical Allele Identifier: CA1674710961

Gene: NOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155427861T= , CM000668.2:g.155427861T=	GRCh38
NC_000006.11:g.155748995T= , CM000668.1:g.155748995T=	GRCh37
NC_000006.10:g.155790687T=	NCBI36
NG_011995.1:g.33043A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000159060.3:c.1145+933A= MANE Select	ENSP00000159060.2:n.1145+933A=
ENST00000159060.2:c.1145+933A=	ENSP00000159060.2:n.1145+933A=
NM_015718.2:c.1145+933A=	NP_056533.1:n.1145+933A=
NM_015718.3:c.1145+933A= MANE Select	NP_056533.1:n.1145+933A=