Canonical Allele Identifier: CA526366296
Gene: NPR1 HGNC NCBI

Linked Data

dbSNP Id: rs1181817918
gnomAD v2: 1-153656597-G-C
gnomAD v3: 1-153684121-G-C
gnomAD v4: 1-153684121-G-C
MyVariant Identifiers: chr1:g.153656597G>C (hg19) chr1:g.153684121G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153684121G>C , CM000663.2:g.153684121G>C GRCh38
NC_000001.10:g.153656597G>C , CM000663.1:g.153656597G>C GRCh37
NC_000001.9:g.151923221G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368680.4:c.1484+297G>C MANE Select ENSP00000357669.3:n.1484+297G>C
ENST00000368680.3:c.1484+297G>C ENSP00000357669.3:n.1484+297G>C
NM_000906.3:c.1484+297G>C NP_000897.3:n.1484+297G>C
XM_005245218.1:c.1484+297G>C XP_005245275.1:n.1484+297G>C
XM_006711342.1:c.1484+297G>C XP_006711405.1:n.1484+297G>C
XM_006711343.1:c.1484+297G>C XP_006711406.1:n.1484+297G>C
XM_011509585.1:c.1484+297G>C XP_011507887.1:n.1484+297G>C
XM_005245218.2:c.1484+297G>C XP_005245275.1:n.1484+297G>C
XM_017001374.2:c.1484+297G>C XP_016856863.1:n.1484+297G>C
NM_000906.4:c.1484+297G>C MANE Select NP_000897.3:n.1484+297G>C
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