Canonical Allele Identifier: CA369857245
Gene: NOS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151001587C>T , CM000669.2:g.151001587C>T GRCh38
NC_000007.13:g.150698675C>T , CM000669.1:g.150698675C>T GRCh37
NC_000007.12:g.150329608C>T NCBI36
NG_011992.1:g.15529C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.1472C>T MANE Select ENSP00000297494.3:p.Thr491Ile
ENST00000297494.7:c.1472C>T ENSP00000297494.3:p.Thr491Ile
ENST00000461406.5:c.854C>T ENSP00000417143.1:p.Thr285Ile
ENST00000467517.1:c.1472C>T ENSP00000420551.1:p.Thr491Ile
ENST00000484524.5:c.1472C>T ENSP00000420215.1:p.Thr491Ile
NM_000603.4:c.1472C>T NP_000594.2:p.Thr491Ile
NM_001160109.1:c.1472C>T NP_001153581.1:p.Thr491Ile
NM_001160110.1:c.1472C>T NP_001153582.1:p.Thr491Ile
NM_001160111.1:c.1472C>T NP_001153583.1:p.Thr491Ile
XM_006716002.2:c.1472C>T XP_006716065.1:p.Thr491Ile
NM_000603.5:c.1472C>T MANE Select NP_000594.2:p.Thr491Ile
NM_001160109.2:c.1472C>T NP_001153581.1:p.Thr491Ile