Canonical Allele Identifier: CA169098481
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs898455162
gnomAD v3: 7-150993070-G-A
gnomAD v4: 7-150993070-G-A
MyVariant Identifiers: chr7:g.150690158G>A (hg19) chr7:g.150993070G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150993070G>A , CM000669.2:g.150993070G>A GRCh38
NC_000007.13:g.150690158G>A , CM000669.1:g.150690158G>A GRCh37
NC_000007.12:g.150321091G>A NCBI36
NG_011992.1:g.7012G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.-51-683G>A MANE Select ENSP00000297494.3:n.-51-683G>A
ENST00000297494.7:c.-51-683G>A ENSP00000297494.3:n.-51-683G>A
ENST00000461406.5:c.-149+1770G>A ENSP00000417143.1:n.-149+1770G>A
NM_000603.4:c.-51-683G>A NP_000594.2:n.-51-683G>A
NM_000603.5:c.-51-683G>A MANE Select NP_000594.2:n.-51-683G>A
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