Canonical Allele Identifier: CA2605591477
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs2117093690
gnomAD v3: 7-150992943-T-G
gnomAD v4: 7-150992943-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992943T>G , CM000669.2:g.150992943T>G GRCh38
NC_000007.13:g.150690031T>G , CM000669.1:g.150690031T>G GRCh37
NC_000007.12:g.150320964T>G NCBI36
NG_011992.1:g.6885T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-810T>G MANE Select ENSP00000297494.3:n.-51-810T>G
ENST00000297494.7:c.-51-810T>G ENSP00000297494.3:n.-51-810T>G
ENST00000461406.5:c.-149+1643T>G ENSP00000417143.1:n.-149+1643T>G
NM_000603.4:c.-51-810T>G NP_000594.2:n.-51-810T>G
NM_000603.5:c.-51-810T>G MANE Select NP_000594.2:n.-51-810T>G
Search 100 bp 5'
Search 100 bp 3'