Canonical Allele Identifier: CA2739316626
Gene: NOS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150993018C>G , CM000669.2:g.150993018C>G GRCh38
NC_000007.13:g.150690106C>G , CM000669.1:g.150690106C>G GRCh37
NC_000007.12:g.150321039C>G NCBI36
NG_011992.1:g.6960C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.-51-735C>G MANE Select ENSP00000297494.3:n.-51-735C>G
ENST00000297494.7:c.-51-735C>G ENSP00000297494.3:n.-51-735C>G
ENST00000461406.5:c.-149+1718C>G ENSP00000417143.1:n.-149+1718C>G
NM_000603.4:c.-51-735C>G NP_000594.2:n.-51-735C>G
NM_000603.5:c.-51-735C>G MANE Select NP_000594.2:n.-51-735C>G