Canonical Allele Identifier: CA1752467266
Gene: NOS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150993053C= , CM000669.2:g.150993053C= GRCh38
NC_000007.13:g.150690141C= , CM000669.1:g.150690141C= GRCh37
NC_000007.12:g.150321074C= NCBI36
NG_011992.1:g.6995C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-700C= MANE Select ENSP00000297494.3:n.-51-700C=
ENST00000297494.7:c.-51-700C= ENSP00000297494.3:n.-51-700C=
ENST00000461406.5:c.-149+1753C= ENSP00000417143.1:n.-149+1753C=
NM_000603.4:c.-51-700C= NP_000594.2:n.-51-700C=
NM_000603.5:c.-51-700C= MANE Select NP_000594.2:n.-51-700C=
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