Canonical Allele Identifier: CA116846746
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs554502766
gnomAD v2: 5-32689845-T-G
gnomAD v3: 5-32689739-T-G
gnomAD v4: 5-32689739-T-G
MyVariant Identifiers: chr5:g.32689845T>G (hg19) chr5:g.32689739T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32689739T>G , CM000667.2:g.32689739T>G GRCh38
NC_000005.9:g.32689845T>G , CM000667.1:g.32689845T>G GRCh37
NC_000005.8:g.32725602T>G NCBI36
NG_028162.2:g.5664T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509104.5:c.100+553T>G ENSP00000425325.1:n.100+553T>G
XM_011514047.1:c.100+553T>G XP_011512349.1:n.100+553T>G
XM_011514047.2:c.100+553T>G XP_011512349.1:n.100+553T>G
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