Canonical Allele Identifier: CA1752446707

Gene: NOS3

Linked Data

• dbSNP Id: rs1795166326

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151003877A>C , CM000669.2:g.151003877A>C	GRCh38
NC_000007.13:g.150700965A>C , CM000669.1:g.150700965A>C	GRCh37
NC_000007.12:g.150331898A>C	NCBI36
NG_011992.1:g.17819A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000297494.8:c.1752+1573A>C MANE Select	ENSP00000297494.3:n.1752+1573A>C
ENST00000297494.7:c.1752+1573A>C	ENSP00000297494.3:n.1752+1573A>C
ENST00000461406.5:c.1134+1573A>C	ENSP00000417143.1:n.1134+1573A>C
ENST00000467517.1:c.2319A>C	ENSP00000420551.1:n.2319A>C
ENST00000484524.5:c.2479A>C	ENSP00000420215.1:n.2479A>C
NM_000603.4:c.1752+1573A>C	NP_000594.2:n.1752+1573A>C
NM_001160109.1:c.1973A>C	NP_001153581.1:n.1973A>C
NM_001160110.1:c.2319A>C	NP_001153582.1:n.2319A>C
NM_001160111.1:c.2479A>C	NP_001153583.1:n.2479A>C
XM_006716002.2:c.1752+1573A>C	XP_006716065.1:n.1752+1573A>C
NM_000603.5:c.1752+1573A>C MANE Select	NP_000594.2:n.1752+1573A>C
NM_001160109.2:c.*182A>C	NP_001153581.1:n.*182A>C