Canonical Allele Identifier: CA169098352

Gene: NOS3

Linked Data

• dbSNP Id: rs1038940989
• MyVariant Identifiers: chr7:g.150689946C>T (hg19) ; chr7:g.150992858C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992858C>T , CM000669.2:g.150992858C>T	GRCh38
NC_000007.13:g.150689946C>T , CM000669.1:g.150689946C>T	GRCh37
NC_000007.12:g.150320879C>T	NCBI36
NG_011992.1:g.6800C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297494.8:c.-51-895C>T MANE Select	ENSP00000297494.3:n.-51-895C>T
ENST00000297494.7:c.-51-895C>T	ENSP00000297494.3:n.-51-895C>T
ENST00000461406.5:c.-149+1558C>T	ENSP00000417143.1:n.-149+1558C>T
NM_000603.4:c.-51-895C>T	NP_000594.2:n.-51-895C>T
NM_000603.5:c.-51-895C>T MANE Select	NP_000594.2:n.-51-895C>T