Canonical Allele Identifier: CA169098284
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1057184401

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992768C>G , CM000669.2:g.150992768C>G GRCh38
NC_000007.13:g.150689856C>G , CM000669.1:g.150689856C>G GRCh37
NC_000007.12:g.150320789C>G NCBI36
NG_011992.1:g.6710C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-51-985C>G MANE Select ENSP00000297494.3:n.-51-985C>G
ENST00000297494.7:c.-51-985C>G ENSP00000297494.3:n.-51-985C>G
ENST00000461406.5:c.-149+1468C>G ENSP00000417143.1:n.-149+1468C>G
NM_000603.4:c.-51-985C>G NP_000594.2:n.-51-985C>G
NM_000603.5:c.-51-985C>G MANE Select NP_000594.2:n.-51-985C>G