Canonical Allele Identifier: CA1752467265
Gene: NOS3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150993049G= , CM000669.2:g.150993049G= GRCh38
NC_000007.13:g.150690137G= , CM000669.1:g.150690137G= GRCh37
NC_000007.12:g.150321070G= NCBI36
NG_011992.1:g.6991G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.-51-704G= MANE Select ENSP00000297494.3:n.-51-704G=
ENST00000297494.7:c.-51-704G= ENSP00000297494.3:n.-51-704G=
ENST00000461406.5:c.-149+1749G= ENSP00000417143.1:n.-149+1749G=
NM_000603.4:c.-51-704G= NP_000594.2:n.-51-704G=
NM_000603.5:c.-51-704G= MANE Select NP_000594.2:n.-51-704G=
Search 100 bp 5'
Search 100 bp 3'