Canonical Allele Identifier: CA458872589
Gene: NOS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150707991G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010903G>C , CM000669.2:g.151010903G>C GRCh38
NC_000007.13:g.150707991G>C , CM000669.1:g.150707991G>C GRCh37
NC_000007.12:g.150338924G>C NCBI36
NG_011992.1:g.24845G>C
NG_030317.1:g.18597C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2901G>C MANE Select ENSP00000297494.3:p.Gly967=
ENST00000297494.7:c.2901G>C ENSP00000297494.3:p.Gly967=
ENST00000461406.5:c.2283G>C ENSP00000417143.1:p.Gly761=
ENST00000468293.5:n.384G>C
ENST00000475017.1:c.782G>C
ENST00000477227.1:n.280G>C
NM_000603.4:c.2901G>C NP_000594.2:p.Gly967=
NM_000603.5:c.2901G>C MANE Select NP_000594.2:p.Gly967=
Search 100 bp 5'
Search 100 bp 3'