Canonical Allele Identifier: CA31691852
Gene: NOS1AP HGNC NCBI

Linked Data

dbSNP Id: rs928807336
MyVariant Identifiers: chr1:g.162169338C>G (hg19) chr1:g.162199548C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162199548C>G , CM000663.2:g.162199548C>G GRCh38
NC_000001.10:g.162169338C>G , CM000663.1:g.162169338C>G GRCh37
NC_000001.9:g.160435962C>G NCBI36
NG_015979.1:g.134758C>G
NG_015979.2:g.134758C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361897.10:c.177+45072C>G MANE Select ENSP00000355133.5:n.177+45072C>G
ENST00000361897.9:c.177+45072C>G ENSP00000355133.5:n.177+45072C>G
ENST00000430120.3:c.177+45072C>G ENSP00000396713.3:n.177+45072C>G
ENST00000530878.5:c.177+45072C>G ENSP00000431586.1:n.177+45072C>G
NM_001164757.1:c.177+45072C>G NP_001158229.1:n.177+45072C>G
NM_014697.2:c.177+45072C>G NP_055512.1:n.177+45072C>G
NM_014697.3:c.177+45072C>G MANE Select NP_055512.1:n.177+45072C>G
NM_001164757.2:c.177+45072C>G NP_001158229.1:n.177+45072C>G
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