Canonical Allele Identifier: CA607800315
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1227827128

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439590G>A , CM000674.2:g.117439590G>A GRCh38
NC_000012.11:g.117877395G>A , CM000674.1:g.117877395G>A GRCh37
NC_000012.10:g.116361778G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000549189.1:n.470+12111C>T