Canonical Allele Identifier: CA2685613471
Gene: NOS3 HGNC NCBI

Linked Data

gnomAD v4: 7-151011019-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151011019C>T , CM000669.2:g.151011019C>T GRCh38
NC_000007.13:g.150708107C>T , CM000669.1:g.150708107C>T GRCh37
NC_000007.12:g.150339040C>T NCBI36
NG_011992.1:g.24961C>T
NG_030317.1:g.18481G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.2984+33C>T MANE Select ENSP00000297494.3:n.2984+33C>T
ENST00000297494.7:c.2984+33C>T ENSP00000297494.3:n.2984+33C>T
ENST00000461406.5:c.2366+33C>T ENSP00000417143.1:n.2366+33C>T
ENST00000468293.5:n.467+33C>T
ENST00000475017.1:c.865+33C>T
ENST00000477227.1:n.363+33C>T
NM_000603.4:c.2984+33C>T NP_000594.2:n.2984+33C>T
NM_000603.5:c.2984+33C>T MANE Select NP_000594.2:n.2984+33C>T
Search 100 bp 5'
Search 100 bp 3'