Canonical Allele Identifier: CA1537629882
Gene: NPR3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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