Canonical Allele Identifier: CA1474562168
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007797C= , CM000666.2:g.88007797C= GRCh38
NC_000004.11:g.88928949C= , CM000666.1:g.88928949C= GRCh37
NC_000004.10:g.89147973C= NCBI36
NG_008604.1:g.5130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.64C= MANE Select ENSP00000237596.2:p.Arg22=
ENST00000237596.6:c.64C= ENSP00000237596.2:p.Arg22=
NM_000297.3:c.64C= NP_000288.1:p.Arg22=
XM_011532028.1:c.64C= XP_011530330.1:p.Arg22=
XR_244632.2:n.159C=
NR_156488.1:n.151C=
XM_011532028.2:c.64C= XP_011530330.1:p.Arg22=
NM_000297.4:c.64C= MANE Select NP_000288.1:p.Arg22=
NR_156488.2:n.163C=