Canonical Allele Identifier: CA4566794

Gene: NOS3

Linked Data

• dbSNP Id: rs772821149
• ExAC: 7:150696133 C / T
• gnomAD v2: 7-150696133-C-T
• gnomAD v4: 7-150999045-C-T
• MyVariant Identifiers: chr7:g.150696133C>T (hg19) ; chr7:g.150999045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150999045C>T , CM000669.2:g.150999045C>T	GRCh38
NC_000007.13:g.150696133C>T , CM000669.1:g.150696133C>T	GRCh37
NC_000007.12:g.150327066C>T	NCBI36
NG_011992.1:g.12987C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297494.8:c.916C>T MANE Select	ENSP00000297494.3:p.Pro306Ser
ENST00000297494.7:c.916C>T	ENSP00000297494.3:p.Pro306Ser
ENST00000461406.5:c.298C>T	ENSP00000417143.1:p.Pro100Ser
ENST00000467517.1:c.916C>T	ENSP00000420551.1:p.Pro306Ser
ENST00000484524.5:c.916C>T	ENSP00000420215.1:p.Pro306Ser
NM_000603.4:c.916C>T	NP_000594.2:p.Pro306Ser
NM_001160109.1:c.916C>T	NP_001153581.1:p.Pro306Ser
NM_001160110.1:c.916C>T	NP_001153582.1:p.Pro306Ser
NM_001160111.1:c.916C>T	NP_001153583.1:p.Pro306Ser
XM_006716002.2:c.916C>T	XP_006716065.1:p.Pro306Ser
NM_000603.5:c.916C>T MANE Select	NP_000594.2:p.Pro306Ser
NM_001160109.2:c.916C>T	NP_001153581.1:p.Pro306Ser