Canonical Allele Identifier: CA369857238
Gene: NOS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151001584T>C , CM000669.2:g.151001584T>C GRCh38
NC_000007.13:g.150698672T>C , CM000669.1:g.150698672T>C GRCh37
NC_000007.12:g.150329605T>C NCBI36
NG_011992.1:g.15526T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.1469T>C MANE Select ENSP00000297494.3:p.Ile490Thr
ENST00000297494.7:c.1469T>C ENSP00000297494.3:p.Ile490Thr
ENST00000461406.5:c.851T>C ENSP00000417143.1:p.Ile284Thr
ENST00000467517.1:c.1469T>C ENSP00000420551.1:p.Ile490Thr
ENST00000484524.5:c.1469T>C ENSP00000420215.1:p.Ile490Thr
NM_000603.4:c.1469T>C NP_000594.2:p.Ile490Thr
NM_001160109.1:c.1469T>C NP_001153581.1:p.Ile490Thr
NM_001160110.1:c.1469T>C NP_001153582.1:p.Ile490Thr
NM_001160111.1:c.1469T>C NP_001153583.1:p.Ile490Thr
XM_006716002.2:c.1469T>C XP_006716065.1:p.Ile490Thr
NM_000603.5:c.1469T>C MANE Select NP_000594.2:p.Ile490Thr
NM_001160109.2:c.1469T>C NP_001153581.1:p.Ile490Thr