Canonical Allele Identifier: CA1752467072

Gene: NOS3

Linked Data

• dbSNP Id: rs1802276564

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150992617_150992618insGCC , CM000669.2:g.150992617_150992618insGCC	GRCh38
NC_000007.13:g.150689705_150689706insGCC , CM000669.1:g.150689705_150689706insGCC	GRCh37
NC_000007.12:g.150320638_150320639insGCC	NCBI36
NG_011992.1:g.6559_6560insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297494.8:c.-51-1136_-51-1135insGCC MANE Select	ENSP00000297494.3:n.-51-1136_-51-1135insGCC
ENST00000297494.7:c.-51-1136_-51-1135insGCC	ENSP00000297494.3:n.-51-1136_-51-1135insGCC
ENST00000461406.5:c.-149+1317_-149+1318insGCC	ENSP00000417143.1:n.-149+1317_-149+1318insGCC
NM_000603.4:c.-51-1136_-51-1135insGCC	NP_000594.2:n.-51-1136_-51-1135insGCC
NM_000603.5:c.-51-1136_-51-1135insGCC MANE Select	NP_000594.2:n.-51-1136_-51-1135insGCC