Canonical Allele Identifier: CA952313466
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439765G>A , CM000674.2:g.117439765G>A GRCh38
NC_000012.11:g.117877570G>A , CM000674.1:g.117877570G>A GRCh37
NC_000012.10:g.116361953G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+11936C>T