Canonical Allele Identifier: CA1537629869
Gene: NPR3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000509104.5:c.100+481G= ENSP00000425325.1:n.100+481G=
XM_011514047.1:c.100+481G= XP_011512349.1:n.100+481G=
XM_011514047.2:c.100+481G= XP_011512349.1:n.100+481G=