Canonical Allele Identifier: CA684138771
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1482937931

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439688C>T , CM000674.2:g.117439688C>T GRCh38
NC_000012.11:g.117877493C>T , CM000674.1:g.117877493C>T GRCh37
NC_000012.10:g.116361876C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12013G>A