Canonical Allele Identifier: CA2513497122
Gene: NOS3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992459C>A , CM000669.2:g.150992459C>A GRCh38
NC_000007.13:g.150689547C>A , CM000669.1:g.150689547C>A GRCh37
NC_000007.12:g.150320480C>A NCBI36
NG_011992.1:g.6401C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-52+1159C>A MANE Select ENSP00000297494.3:n.-52+1159C>A
ENST00000297494.7:c.-52+1159C>A ENSP00000297494.3:n.-52+1159C>A
ENST00000461406.5:c.-149+1159C>A ENSP00000417143.1:n.-149+1159C>A
NM_000603.4:c.-52+1159C>A NP_000594.2:n.-52+1159C>A
NM_000603.5:c.-52+1159C>A MANE Select NP_000594.2:n.-52+1159C>A
Search 100 bp 5'
Search 100 bp 3'