Canonical Allele Identifier: CA1108714815
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1802288749
gnomAD v3: 7-150993068-G-C
gnomAD v4: 7-150993068-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150993068G>C , CM000669.2:g.150993068G>C GRCh38
NC_000007.13:g.150690156G>C , CM000669.1:g.150690156G>C GRCh37
NC_000007.12:g.150321089G>C NCBI36
NG_011992.1:g.7010G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-685G>C MANE Select ENSP00000297494.3:n.-51-685G>C
ENST00000297494.7:c.-51-685G>C ENSP00000297494.3:n.-51-685G>C
ENST00000461406.5:c.-149+1768G>C ENSP00000417143.1:n.-149+1768G>C
NM_000603.4:c.-51-685G>C NP_000594.2:n.-51-685G>C
NM_000603.5:c.-51-685G>C MANE Select NP_000594.2:n.-51-685G>C
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