Canonical Allele Identifier: CA458872596
Gene: NOS3 HGNC NCBI

Linked Data

gnomAD v4: 7-151010909-C-T
MyVariant Identifiers: chr7:g.150707997C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010909C>T , CM000669.2:g.151010909C>T GRCh38
NC_000007.13:g.150707997C>T , CM000669.1:g.150707997C>T GRCh37
NC_000007.12:g.150338930C>T NCBI36
NG_011992.1:g.24851C>T
NG_030317.1:g.18591G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2907C>T MANE Select ENSP00000297494.3:p.Gly969=
ENST00000297494.7:c.2907C>T ENSP00000297494.3:p.Gly969=
ENST00000461406.5:c.2289C>T ENSP00000417143.1:p.Gly763=
ENST00000468293.5:n.390C>T
ENST00000475017.1:c.788C>T
ENST00000477227.1:n.286C>T
NM_000603.4:c.2907C>T NP_000594.2:p.Gly969=
NM_000603.5:c.2907C>T MANE Select NP_000594.2:p.Gly969=
Search 100 bp 5'
Search 100 bp 3'