Canonical Allele Identifier: CA2066046128
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1870088207

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439605C>T , CM000674.2:g.117439605C>T GRCh38
NC_000012.11:g.117877410C>T , CM000674.1:g.117877410C>T GRCh37
NC_000012.10:g.116361793C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12096G>A