Canonical Allele Identifier: CA169098150
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs2566519
MyVariant Identifiers: chr7:g.150689591C>G (hg19) chr7:g.150992503C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992503C>G , CM000669.2:g.150992503C>G GRCh38
NC_000007.13:g.150689591C>G , CM000669.1:g.150689591C>G GRCh37
NC_000007.12:g.150320524C>G NCBI36
NG_011992.1:g.6445C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-52+1203C>G MANE Select ENSP00000297494.3:n.-52+1203C>G
ENST00000297494.7:c.-52+1203C>G ENSP00000297494.3:n.-52+1203C>G
ENST00000461406.5:c.-149+1203C>G ENSP00000417143.1:n.-149+1203C>G
NM_000603.4:c.-52+1203C>G NP_000594.2:n.-52+1203C>G
NM_000603.5:c.-52+1203C>G MANE Select NP_000594.2:n.-52+1203C>G
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