Canonical Allele Identifier: CA1752467048
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992550G= , CM000669.2:g.150992550G= GRCh38
NC_000007.13:g.150689638G= , CM000669.1:g.150689638G= GRCh37
NC_000007.12:g.150320571G= NCBI36
NG_011992.1:g.6492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-1203G= MANE Select ENSP00000297494.3:n.-51-1203G=
ENST00000297494.7:c.-51-1203G= ENSP00000297494.3:n.-51-1203G=
ENST00000461406.5:c.-149+1250G= ENSP00000417143.1:n.-149+1250G=
NM_000603.4:c.-51-1203G= NP_000594.2:n.-51-1203G=
NM_000603.5:c.-51-1203G= MANE Select NP_000594.2:n.-51-1203G=