Canonical Allele Identifier: CA1537629880
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1740342608

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32689690A>G , CM000667.2:g.32689690A>G GRCh38
NC_000005.9:g.32689796A>G , CM000667.1:g.32689796A>G GRCh37
NC_000005.8:g.32725553A>G NCBI36
NG_028162.2:g.5615A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509104.5:c.100+504A>G ENSP00000425325.1:n.100+504A>G
XM_011514047.1:c.100+504A>G XP_011512349.1:n.100+504A>G
XM_011514047.2:c.100+504A>G XP_011512349.1:n.100+504A>G