Canonical Allele Identifier: CA890267990
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs1304487355
gnomAD v3: 1-162199549-C-A
gnomAD v4: 1-162199549-C-A
MyVariant Identifiers: chr1:g.162169339C>A (hg19) chr1:g.162199549C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199549C>A , CM000663.2:g.162199549C>A GRCh38
NC_000001.10:g.162169339C>A , CM000663.1:g.162169339C>A GRCh37
NC_000001.9:g.160435963C>A NCBI36
NG_015979.1:g.134759C>A
NG_015979.2:g.134759C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+45073C>A MANE Select ENSP00000355133.5:n.177+45073C>A
ENST00000361897.9:c.177+45073C>A ENSP00000355133.5:n.177+45073C>A
ENST00000430120.3:c.177+45073C>A ENSP00000396713.3:n.177+45073C>A
ENST00000530878.5:c.177+45073C>A ENSP00000431586.1:n.177+45073C>A
NM_001164757.1:c.177+45073C>A NP_001158229.1:n.177+45073C>A
NM_014697.2:c.177+45073C>A NP_055512.1:n.177+45073C>A
NM_014697.3:c.177+45073C>A MANE Select NP_055512.1:n.177+45073C>A
NM_001164757.2:c.177+45073C>A NP_001158229.1:n.177+45073C>A
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