Canonical Allele Identifier: CA1537629883
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1740342655
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32689692C>T , CM000667.2:g.32689692C>T GRCh38
NC_000005.9:g.32689798C>T , CM000667.1:g.32689798C>T GRCh37
NC_000005.8:g.32725555C>T NCBI36
NG_028162.2:g.5617C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509104.5:c.100+506C>T ENSP00000425325.1:n.100+506C>T
XM_011514047.1:c.100+506C>T XP_011512349.1:n.100+506C>T
XM_011514047.2:c.100+506C>T XP_011512349.1:n.100+506C>T
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