Canonical Allele Identifier: CA2778426719

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992897C>T , CM000669.2:g.150992897C>T	GRCh38
NC_000007.13:g.150689985C>T , CM000669.1:g.150689985C>T	GRCh37
NC_000007.12:g.150320918C>T	NCBI36
NG_011992.1:g.6839C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-856C>T MANE Select	ENSP00000297494.3:n.-51-856C>T
ENST00000297494.7:c.-51-856C>T	ENSP00000297494.3:n.-51-856C>T
ENST00000461406.5:c.-149+1597C>T	ENSP00000417143.1:n.-149+1597C>T
NM_000603.4:c.-51-856C>T	NP_000594.2:n.-51-856C>T
NM_000603.5:c.-51-856C>T MANE Select	NP_000594.2:n.-51-856C>T