Canonical Allele Identifier: CA12097448
Gene: NPR3 HGNC NCBI

Linked Data

dbSNP Id: rs7729447
gnomAD v2: 5-32689773-G-A
gnomAD v3: 5-32689667-G-A
gnomAD v4: 5-32689667-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32689667G>A , CM000667.2:g.32689667G>A GRCh38
NC_000005.9:g.32689773G>A , CM000667.1:g.32689773G>A GRCh37
NC_000005.8:g.32725530G>A NCBI36
NG_028162.2:g.5592G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509104.5:c.100+481G>A ENSP00000425325.1:n.100+481G>A
XM_011514047.1:c.100+481G>A XP_011512349.1:n.100+481G>A
XM_011514047.2:c.100+481G>A XP_011512349.1:n.100+481G>A