Canonical Allele Identifier: CA2066036876
Gene: NOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1010238506
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117342576T>C , CM000674.2:g.117342576T>C GRCh38
NC_000012.11:g.117780381T>C , CM000674.1:g.117780381T>C GRCh37
NC_000012.10:g.116264764T>C NCBI36
NG_011991.2:g.24202A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000317775.11:c.-420-11087A>G MANE Select ENSP00000320758.6:n.-420-11087A>G
ENST00000317775.10:c.-420-11087A>G ENSP00000320758.6:n.-420-11087A>G
ENST00000549189.1:n.471-11087A>G
ENST00000618760.4:c.-420-11087A>G ENSP00000477999.1:n.-420-11087A>G
NM_000620.4:c.-420-11087A>G NP_000611.1:n.-420-11087A>G
NM_001204218.1:c.-420-11087A>G NP_001191147.1:n.-420-11087A>G
XM_011538398.1:c.-420-11087A>G XP_011536700.1:n.-420-11087A>G
NM_000620.5:c.-420-11087A>G MANE Select NP_000611.1:n.-420-11087A>G
NM_001204218.2:c.-420-11087A>G NP_001191147.1:n.-420-11087A>G
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