Canonical Allele Identifier: CA1108714814
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1802288683
gnomAD v3: 7-150993067-G-T
gnomAD v4: 7-150993067-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150993067G>T , CM000669.2:g.150993067G>T GRCh38
NC_000007.13:g.150690155G>T , CM000669.1:g.150690155G>T GRCh37
NC_000007.12:g.150321088G>T NCBI36
NG_011992.1:g.7009G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-686G>T MANE Select ENSP00000297494.3:n.-51-686G>T
ENST00000297494.7:c.-51-686G>T ENSP00000297494.3:n.-51-686G>T
ENST00000461406.5:c.-149+1767G>T ENSP00000417143.1:n.-149+1767G>T
NM_000603.4:c.-51-686G>T NP_000594.2:n.-51-686G>T
NM_000603.5:c.-51-686G>T MANE Select NP_000594.2:n.-51-686G>T
Search 100 bp 5'
Search 100 bp 3'