Canonical Allele Identifier: CA1752467149
Gene: NOS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992771A= , CM000669.2:g.150992771A= GRCh38
NC_000007.13:g.150689859A= , CM000669.1:g.150689859A= GRCh37
NC_000007.12:g.150320792A= NCBI36
NG_011992.1:g.6713A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-982A= MANE Select ENSP00000297494.3:n.-51-982A=
ENST00000297494.7:c.-51-982A= ENSP00000297494.3:n.-51-982A=
ENST00000461406.5:c.-149+1471A= ENSP00000417143.1:n.-149+1471A=
NM_000603.4:c.-51-982A= NP_000594.2:n.-51-982A=
NM_000603.5:c.-51-982A= MANE Select NP_000594.2:n.-51-982A=
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