Canonical Allele Identifier: CA835224104
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1470279311
gnomAD v3: 7-150992998-C-A
gnomAD v4: 7-150992998-C-A
MyVariant Identifiers: chr7:g.150690086C>A (hg19) chr7:g.150992998C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992998C>A , CM000669.2:g.150992998C>A GRCh38
NC_000007.13:g.150690086C>A , CM000669.1:g.150690086C>A GRCh37
NC_000007.12:g.150321019C>A NCBI36
NG_011992.1:g.6940C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.-51-755C>A MANE Select ENSP00000297494.3:n.-51-755C>A
ENST00000297494.7:c.-51-755C>A ENSP00000297494.3:n.-51-755C>A
ENST00000461406.5:c.-149+1698C>A ENSP00000417143.1:n.-149+1698C>A
NM_000603.4:c.-51-755C>A NP_000594.2:n.-51-755C>A
NM_000603.5:c.-51-755C>A MANE Select NP_000594.2:n.-51-755C>A
Search 100 bp 5'
Search 100 bp 3'