Canonical Allele Identifier: CA1752467229
Gene: NOS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992958T= , CM000669.2:g.150992958T= GRCh38
NC_000007.13:g.150690046T= , CM000669.1:g.150690046T= GRCh37
NC_000007.12:g.150320979T= NCBI36
NG_011992.1:g.6900T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-795T= MANE Select ENSP00000297494.3:n.-51-795T=
ENST00000297494.7:c.-51-795T= ENSP00000297494.3:n.-51-795T=
ENST00000461406.5:c.-149+1658T= ENSP00000417143.1:n.-149+1658T=
NM_000603.4:c.-51-795T= NP_000594.2:n.-51-795T=
NM_000603.5:c.-51-795T= MANE Select NP_000594.2:n.-51-795T=
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