Canonical Allele Identifier: CA1752467097
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1243548554

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992637A>G , CM000669.2:g.150992637A>G GRCh38
NC_000007.13:g.150689725A>G , CM000669.1:g.150689725A>G GRCh37
NC_000007.12:g.150320658A>G NCBI36
NG_011992.1:g.6579A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-1116A>G MANE Select ENSP00000297494.3:n.-51-1116A>G
ENST00000297494.7:c.-51-1116A>G ENSP00000297494.3:n.-51-1116A>G
ENST00000461406.5:c.-149+1337A>G ENSP00000417143.1:n.-149+1337A>G
NM_000603.4:c.-51-1116A>G NP_000594.2:n.-51-1116A>G
NM_000603.5:c.-51-1116A>G MANE Select NP_000594.2:n.-51-1116A>G