Canonical Allele Identifier: CA2685607969

Gene: NOS3

Linked Data

• gnomAD v4: 7-151003783-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151003783T>C , CM000669.2:g.151003783T>C	GRCh38
NC_000007.13:g.150700871T>C , CM000669.1:g.150700871T>C	GRCh37
NC_000007.12:g.150331804T>C	NCBI36
NG_011992.1:g.17725T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.1752+1479T>C MANE Select	ENSP00000297494.3:n.1752+1479T>C
ENST00000297494.7:c.1752+1479T>C	ENSP00000297494.3:n.1752+1479T>C
ENST00000461406.5:c.1134+1479T>C	ENSP00000417143.1:n.1134+1479T>C
ENST00000467517.1:c.2225T>C	ENSP00000420551.1:n.2225T>C
ENST00000484524.5:c.2385T>C	ENSP00000420215.1:n.2385T>C
NM_000603.4:c.1752+1479T>C	NP_000594.2:n.1752+1479T>C
NM_001160109.1:c.1879T>C	NP_001153581.1:n.1879T>C
NM_001160110.1:c.2225T>C	NP_001153582.1:n.2225T>C
NM_001160111.1:c.2385T>C	NP_001153583.1:n.2385T>C
XM_006716002.2:c.1752+1479T>C	XP_006716065.1:n.1752+1479T>C
NM_000603.5:c.1752+1479T>C MANE Select	NP_000594.2:n.1752+1479T>C
NM_001160109.2:c.*88T>C	NP_001153581.1:n.*88T>C