Canonical Allele Identifier: CA1118082
Gene: NPR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 932523
ClinVar RCV Id: RCV001200365
dbSNP Id: rs755193080
ExAC: 1:153656268 C / G
gnomAD v2: 1-153656268-C-G
gnomAD v4: 1-153683792-C-G
MyVariant Identifiers: chr1:g.153656268C>G (hg19) chr1:g.153683792C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153683792C>G , CM000663.2:g.153683792C>G GRCh38
NC_000001.10:g.153656268C>G , CM000663.1:g.153656268C>G GRCh37
NC_000001.9:g.151922892C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368680.4:c.1452C>G MANE Select ENSP00000357669.3:p.Leu484=
ENST00000368680.3:c.1452C>G ENSP00000357669.3:p.Leu484=
NM_000906.3:c.1452C>G NP_000897.3:p.Leu484=
XM_005245218.1:c.1452C>G XP_005245275.1:p.Leu484=
XM_006711342.1:c.1452C>G XP_006711405.1:p.Leu484=
XM_006711343.1:c.1452C>G XP_006711406.1:p.Leu484=
XM_011509585.1:c.1452C>G XP_011507887.1:p.Leu484=
XM_005245218.2:c.1452C>G XP_005245275.1:p.Leu484=
XM_017001374.2:c.1452C>G XP_016856863.1:p.Leu484=
NM_000906.4:c.1452C>G MANE Select NP_000897.3:p.Leu484=
Search 100 bp 5'
Search 100 bp 3'