Canonical Allele Identifier: CA1752467196
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992878T= , CM000669.2:g.150992878T= GRCh38
NC_000007.13:g.150689966T= , CM000669.1:g.150689966T= GRCh37
NC_000007.12:g.150320899T= NCBI36
NG_011992.1:g.6820T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-875T= MANE Select ENSP00000297494.3:n.-51-875T=
ENST00000297494.7:c.-51-875T= ENSP00000297494.3:n.-51-875T=
ENST00000461406.5:c.-149+1578T= ENSP00000417143.1:n.-149+1578T=
NM_000603.4:c.-51-875T= NP_000594.2:n.-51-875T=
NM_000603.5:c.-51-875T= MANE Select NP_000594.2:n.-51-875T=