Canonical Allele Identifier: CA369864741
Gene: NOS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150707992C>A (hg19) chr7:g.151010904C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010904C>A , CM000669.2:g.151010904C>A GRCh38
NC_000007.13:g.150707992C>A , CM000669.1:g.150707992C>A GRCh37
NC_000007.12:g.150338925C>A NCBI36
NG_011992.1:g.24846C>A
NG_030317.1:g.18596G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.2902C>A MANE Select ENSP00000297494.3:p.Leu968Met
ENST00000297494.7:c.2902C>A ENSP00000297494.3:p.Leu968Met
ENST00000461406.5:c.2284C>A ENSP00000417143.1:p.Leu762Met
ENST00000468293.5:n.385C>A
ENST00000475017.1:c.783C>A
ENST00000477227.1:n.281C>A
NM_000603.4:c.2902C>A NP_000594.2:p.Leu968Met
NM_000603.5:c.2902C>A MANE Select NP_000594.2:p.Leu968Met
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