Canonical Allele Identifier: CA12525506
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1800779

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992855G>A , CM000669.2:g.150992855G>A GRCh38
NC_000007.13:g.150689943G>A , CM000669.1:g.150689943G>A GRCh37
NC_000007.12:g.150320876G>A NCBI36
NG_011992.1:g.6797G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.-51-898G>A MANE Select ENSP00000297494.3:p.=
ENST00000297494.7:c.-51-898G>A ENSP00000297494.3:p.=
ENST00000461406.5:c.-149+1555G>A ENSP00000417143.1:p.=
NM_000603.4:c.-51-898G>A NP_000594.2:p.=
NM_000603.5:c.-51-898G>A MANE Select NP_000594.2:p.=