Canonical Allele Identifier: CA2539100932
Gene: NOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439603C>A , CM000674.2:g.117439603C>A GRCh38
NC_000012.11:g.117877408C>A , CM000674.1:g.117877408C>A GRCh37
NC_000012.10:g.116361791C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12098G>T