Canonical Allele Identifier: CA952281388
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117365710C>G , CM000674.2:g.117365710C>G GRCh38
NC_000012.11:g.117803515C>G , CM000674.1:g.117803515C>G GRCh37
NC_000012.10:g.116287898C>G NCBI36
NG_011991.2:g.1068G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.471-34221G>C