Canonical Allele Identifier: CA835223914
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1243548554
MyVariant Identifiers: chr7:g.150689725A>T (hg19) chr7:g.150992637A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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