Canonical Allele Identifier: CA1674710979

Gene: NOX3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.155427891C= , CM000668.2:g.155427891C=	GRCh38
NC_000006.11:g.155749025C= , CM000668.1:g.155749025C=	GRCh37
NC_000006.10:g.155790717C=	NCBI36
NG_011995.1:g.33013G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000159060.3:c.1145+903G= MANE Select	ENSP00000159060.2:n.1145+903G=
ENST00000159060.2:c.1145+903G=	ENSP00000159060.2:n.1145+903G=
NM_015718.2:c.1145+903G=	NP_056533.1:n.1145+903G=
NM_015718.3:c.1145+903G= MANE Select	NP_056533.1:n.1145+903G=