Canonical Allele Identifier: CA1846178142
Community Standard Title: NC_000009.12:g.35766564C=
Gene: NPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35766564C= , CM000671.2:g.35766564C= GRCh38
NC_000009.11:g.35766561C= , CM000671.1:g.35766561C= GRCh37
NC_000009.10:g.35756561C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005251479.3:c.-642-5599C= XP_005251536.1:n.-642-5599C=
XM_011517889.1:c.-1440-5599C= XP_011516191.1:n.-1440-5599C=
XM_011517890.1:c.-1227+9367C= XP_011516192.1:n.-1227+9367C=
XM_011517891.1:c.-1135-5599C= XP_011516193.1:n.-1135-5599C=
XM_011517892.1:c.-1307-5599C= XP_011516194.1:n.-1307-5599C=
XM_011517893.1:c.-1440-5599C= XP_011516195.1:n.-1440-5599C=
XM_011517894.1:c.-1227+9703C= XP_011516196.1:n.-1227+9703C=