Canonical Allele Identifier: CA369864740

Gene: NOS3

Linked Data

• MyVariant Identifiers: chr7:g.150707990G>T (hg19) ; chr7:g.151010902G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151010902G>T , CM000669.2:g.151010902G>T	GRCh38
NC_000007.13:g.150707990G>T , CM000669.1:g.150707990G>T	GRCh37
NC_000007.12:g.150338923G>T	NCBI36
NG_011992.1:g.24844G>T
NG_030317.1:g.18598C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.2900G>T MANE Select	ENSP00000297494.3:p.Gly967Val
ENST00000297494.7:c.2900G>T	ENSP00000297494.3:p.Gly967Val
ENST00000461406.5:c.2282G>T	ENSP00000417143.1:p.Gly761Val
ENST00000468293.5:n.383G>T
ENST00000475017.1:c.781G>T
ENST00000477227.1:n.279G>T
NM_000603.4:c.2900G>T	NP_000594.2:p.Gly967Val
NM_000603.5:c.2900G>T MANE Select	NP_000594.2:p.Gly967Val