Canonical Allele Identifier: CA369864758
Gene: NOS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010913C>G , CM000669.2:g.151010913C>G GRCh38
NC_000007.13:g.150708001C>G , CM000669.1:g.150708001C>G GRCh37
NC_000007.12:g.150338934C>G NCBI36
NG_011992.1:g.24855C>G
NG_030317.1:g.18587G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.2911C>G MANE Select ENSP00000297494.3:p.Leu971Val
ENST00000297494.7:c.2911C>G ENSP00000297494.3:p.Leu971Val
ENST00000461406.5:c.2293C>G ENSP00000417143.1:p.Leu765Val
ENST00000468293.5:n.394C>G
ENST00000475017.1:c.792C>G
ENST00000477227.1:n.290C>G
NM_000603.4:c.2911C>G NP_000594.2:p.Leu971Val
NM_000603.5:c.2911C>G MANE Select NP_000594.2:p.Leu971Val