Canonical Allele Identifier: CA2066046347
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1870091014

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439711G>C , CM000674.2:g.117439711G>C GRCh38
NC_000012.11:g.117877516G>C , CM000674.1:g.117877516G>C GRCh37
NC_000012.10:g.116361899G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+11990C>G