Canonical Allele Identifier: CA30689350
Gene: NPR1 HGNC NCBI

Linked Data

dbSNP Id: rs758556850
gnomAD v2: 1-153656571-G-A
gnomAD v3: 1-153684095-G-A
gnomAD v4: 1-153684095-G-A
MyVariant Identifiers: chr1:g.153656571G>A (hg19) chr1:g.153684095G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153684095G>A , CM000663.2:g.153684095G>A GRCh38
NC_000001.10:g.153656571G>A , CM000663.1:g.153656571G>A GRCh37
NC_000001.9:g.151923195G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368680.4:c.1484+271G>A MANE Select ENSP00000357669.3:n.1484+271G>A
ENST00000368680.3:c.1484+271G>A ENSP00000357669.3:n.1484+271G>A
NM_000906.3:c.1484+271G>A NP_000897.3:n.1484+271G>A
XM_005245218.1:c.1484+271G>A XP_005245275.1:n.1484+271G>A
XM_006711342.1:c.1484+271G>A XP_006711405.1:n.1484+271G>A
XM_006711343.1:c.1484+271G>A XP_006711406.1:n.1484+271G>A
XM_011509585.1:c.1484+271G>A XP_011507887.1:n.1484+271G>A
XM_005245218.2:c.1484+271G>A XP_005245275.1:n.1484+271G>A
XM_017001374.2:c.1484+271G>A XP_016856863.1:n.1484+271G>A
NM_000906.4:c.1484+271G>A MANE Select NP_000897.3:n.1484+271G>A
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