Canonical Allele Identifier: CA169098218
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs986966563
gnomAD v3: 7-150992659-A-G
gnomAD v4: 7-150992659-A-G
MyVariant Identifiers: chr7:g.150992659A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992659A>G , CM000669.2:g.150992659A>G GRCh38
NC_000007.13:g.150689747A>G , CM000669.1:g.150689747A>G GRCh37
NC_000007.12:g.150320680A>G NCBI36
NG_011992.1:g.6601A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-1094A>G MANE Select ENSP00000297494.3:n.-51-1094A>G
ENST00000297494.7:c.-51-1094A>G ENSP00000297494.3:n.-51-1094A>G
ENST00000461406.5:c.-149+1359A>G ENSP00000417143.1:n.-149+1359A>G
NM_000603.4:c.-51-1094A>G NP_000594.2:n.-51-1094A>G
NM_000603.5:c.-51-1094A>G MANE Select NP_000594.2:n.-51-1094A>G
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