Canonical Allele Identifier: CA2066046155
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs920919529
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117439622C>G , CM000674.2:g.117439622C>G GRCh38
NC_000012.11:g.117877427C>G , CM000674.1:g.117877427C>G GRCh37
NC_000012.10:g.116361810C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000549189.1:n.470+12079G>C
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