Canonical Allele Identifier: CA835223862
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1347471544
gnomAD v3: 7-150992494-C-T
gnomAD v4: 7-150992494-C-T
MyVariant Identifiers: chr7:g.150689582C>T (hg19) chr7:g.150992494C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992494C>T , CM000669.2:g.150992494C>T GRCh38
NC_000007.13:g.150689582C>T , CM000669.1:g.150689582C>T GRCh37
NC_000007.12:g.150320515C>T NCBI36
NG_011992.1:g.6436C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-52+1194C>T MANE Select ENSP00000297494.3:n.-52+1194C>T
ENST00000297494.7:c.-52+1194C>T ENSP00000297494.3:n.-52+1194C>T
ENST00000461406.5:c.-149+1194C>T ENSP00000417143.1:n.-149+1194C>T
NM_000603.4:c.-52+1194C>T NP_000594.2:n.-52+1194C>T
NM_000603.5:c.-52+1194C>T MANE Select NP_000594.2:n.-52+1194C>T
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