Canonical Allele Identifier: CA458872374

Gene: NOS3

Linked Data

• dbSNP Id: rs1256519473
• gnomAD v2: 7-150699050-C-T
• gnomAD v4: 7-151001962-C-T
• MyVariant Identifiers: chr7:g.150699050C>T (hg19) ; chr7:g.151001962C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151001962C>T , CM000669.2:g.151001962C>T	GRCh38
NC_000007.13:g.150699050C>T , CM000669.1:g.150699050C>T	GRCh37
NC_000007.12:g.150329983C>T	NCBI36
NG_011992.1:g.15904C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1644C>T MANE Select	ENSP00000297494.3:p.Pro548=
ENST00000297494.7:c.1644C>T	ENSP00000297494.3:p.Pro548=
ENST00000460603.1:n.96C>T
ENST00000461406.5:c.1026C>T	ENSP00000417143.1:p.Pro342=
ENST00000467517.1:c.1644C>T	ENSP00000420551.1:p.Pro548=
ENST00000484524.5:c.1644C>T	ENSP00000420215.1:p.Pro548=
NM_000603.4:c.1644C>T	NP_000594.2:p.Pro548=
NM_001160109.1:c.1644C>T	NP_001153581.1:p.Pro548=
NM_001160110.1:c.1644C>T	NP_001153582.1:p.Pro548=
NM_001160111.1:c.1644C>T	NP_001153583.1:p.Pro548=
XM_006716002.2:c.1644C>T	XP_006716065.1:p.Pro548=
NM_000603.5:c.1644C>T MANE Select	NP_000594.2:p.Pro548=
NM_001160109.2:c.1644C>T	NP_001153581.1:p.Pro548=