Canonical Allele Identifier: CA458872593
Gene: NOS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150707994G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010906G>T , CM000669.2:g.151010906G>T GRCh38
NC_000007.13:g.150707994G>T , CM000669.1:g.150707994G>T GRCh37
NC_000007.12:g.150338927G>T NCBI36
NG_011992.1:g.24848G>T
NG_030317.1:g.18594C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2904G>T MANE Select ENSP00000297494.3:p.Leu968=
ENST00000297494.7:c.2904G>T ENSP00000297494.3:p.Leu968=
ENST00000461406.5:c.2286G>T ENSP00000417143.1:p.Leu762=
ENST00000468293.5:n.387G>T
ENST00000475017.1:c.785G>T
ENST00000477227.1:n.283G>T
NM_000603.4:c.2904G>T NP_000594.2:p.Leu968=
NM_000603.5:c.2904G>T MANE Select NP_000594.2:p.Leu968=
Search 100 bp 5'
Search 100 bp 3'