Canonical Allele Identifier: CA245041523
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs374917717

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439610C>T , CM000674.2:g.117439610C>T GRCh38
NC_000012.11:g.117877415C>T , CM000674.1:g.117877415C>T GRCh37
NC_000012.10:g.116361798C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12091G>A