Canonical Allele Identifier: CA1752440887
Gene: NOS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151011003A= , CM000669.2:g.151011003A= GRCh38
NC_000007.13:g.150708091A= , CM000669.1:g.150708091A= GRCh37
NC_000007.12:g.150339024A= NCBI36
NG_011992.1:g.24945A=
NG_030317.1:g.18497T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.2984+17A= MANE Select ENSP00000297494.3:n.2984+17A=
ENST00000297494.7:c.2984+17A= ENSP00000297494.3:n.2984+17A=
ENST00000461406.5:c.2366+17A= ENSP00000417143.1:n.2366+17A=
ENST00000468293.5:n.467+17A=
ENST00000475017.1:c.865+17A=
ENST00000477227.1:n.363+17A=
NM_000603.4:c.2984+17A= NP_000594.2:n.2984+17A=
NM_000603.5:c.2984+17A= MANE Select NP_000594.2:n.2984+17A=
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