Canonical Allele Identifier: CA116846741
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs973330627
COSMIC: COSN2102793
MyVariant Identifiers: chr5:g.32689782T>C (hg19) chr5:g.32689676T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32689676T>C , CM000667.2:g.32689676T>C GRCh38
NC_000005.9:g.32689782T>C , CM000667.1:g.32689782T>C GRCh37
NC_000005.8:g.32725539T>C NCBI36
NG_028162.2:g.5601T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000509104.5:c.100+490T>C ENSP00000425325.1:n.100+490T>C
XM_011514047.1:c.100+490T>C XP_011512349.1:n.100+490T>C
XM_011514047.2:c.100+490T>C XP_011512349.1:n.100+490T>C
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