Canonical Allele Identifier: CA369864747
Gene: NOS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150707995G>C (hg19) chr7:g.151010907G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151010907G>C , CM000669.2:g.151010907G>C GRCh38
NC_000007.13:g.150707995G>C , CM000669.1:g.150707995G>C GRCh37
NC_000007.12:g.150338928G>C NCBI36
NG_011992.1:g.24849G>C
NG_030317.1:g.18593C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2905G>C MANE Select ENSP00000297494.3:p.Gly969Arg
ENST00000297494.7:c.2905G>C ENSP00000297494.3:p.Gly969Arg
ENST00000461406.5:c.2287G>C ENSP00000417143.1:p.Gly763Arg
ENST00000468293.5:n.388G>C
ENST00000475017.1:c.786G>C
ENST00000477227.1:n.284G>C
NM_000603.4:c.2905G>C NP_000594.2:p.Gly969Arg
NM_000603.5:c.2905G>C MANE Select NP_000594.2:p.Gly969Arg
Search 100 bp 5'
Search 100 bp 3'