Canonical Allele Identifier: CA1752440888

Gene: NOS3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151011004C= , CM000669.2:g.151011004C=	GRCh38
NC_000007.13:g.150708092C= , CM000669.1:g.150708092C=	GRCh37
NC_000007.12:g.150339025C=	NCBI36
NG_011992.1:g.24946C=
NG_030317.1:g.18496G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.2984+18C= MANE Select	ENSP00000297494.3:n.2984+18C=
ENST00000297494.7:c.2984+18C=	ENSP00000297494.3:n.2984+18C=
ENST00000461406.5:c.2366+18C=	ENSP00000417143.1:n.2366+18C=
ENST00000468293.5:n.467+18C=
ENST00000475017.1:c.865+18C=
ENST00000477227.1:n.363+18C=
NM_000603.4:c.2984+18C=	NP_000594.2:n.2984+18C=
NM_000603.5:c.2984+18C= MANE Select	NP_000594.2:n.2984+18C=