Canonical Allele Identifier: CA169098157
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1023069926
gnomAD v3: 7-150992517-T-A
gnomAD v4: 7-150992517-T-A
MyVariant Identifiers: chr7:g.150689605T>A (hg19) chr7:g.150992517T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992517T>A , CM000669.2:g.150992517T>A GRCh38
NC_000007.13:g.150689605T>A , CM000669.1:g.150689605T>A GRCh37
NC_000007.12:g.150320538T>A NCBI36
NG_011992.1:g.6459T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-52+1217T>A MANE Select ENSP00000297494.3:n.-52+1217T>A
ENST00000297494.7:c.-52+1217T>A ENSP00000297494.3:n.-52+1217T>A
ENST00000461406.5:c.-149+1217T>A ENSP00000417143.1:n.-149+1217T>A
NM_000603.4:c.-52+1217T>A NP_000594.2:n.-52+1217T>A
NM_000603.5:c.-52+1217T>A MANE Select NP_000594.2:n.-52+1217T>A
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