Canonical Allele Identifier: CA169098371
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1020737794
gnomAD v2: 7-150690014-A-C
gnomAD v3: 7-150992926-A-C
gnomAD v4: 7-150992926-A-C
MyVariant Identifiers: chr7:g.150690014A>C (hg19) chr7:g.150992926A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992926A>C , CM000669.2:g.150992926A>C GRCh38
NC_000007.13:g.150690014A>C , CM000669.1:g.150690014A>C GRCh37
NC_000007.12:g.150320947A>C NCBI36
NG_011992.1:g.6868A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-827A>C MANE Select ENSP00000297494.3:n.-51-827A>C
ENST00000297494.7:c.-51-827A>C ENSP00000297494.3:n.-51-827A>C
ENST00000461406.5:c.-149+1626A>C ENSP00000417143.1:n.-149+1626A>C
NM_000603.4:c.-51-827A>C NP_000594.2:n.-51-827A>C
NM_000603.5:c.-51-827A>C MANE Select NP_000594.2:n.-51-827A>C
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