Canonical Allele Identifier: CA1474562363
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008153G= , CM000666.2:g.88008153G= GRCh38
NC_000004.11:g.88929305G= , CM000666.1:g.88929305G= GRCh37
NC_000004.10:g.89148329G= NCBI36
NG_008604.1:g.5486G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.420G= MANE Select ENSP00000237596.2:p.Gly140=
ENST00000237596.6:c.420G= ENSP00000237596.2:p.Gly140=
NM_000297.3:c.420G= NP_000288.1:p.Gly140=
XM_011532028.1:c.420G= XP_011530330.1:p.Gly140=
XR_244632.2:n.515G=
NR_156488.1:n.507G=
XM_011532028.2:c.420G= XP_011530330.1:p.Gly140=
NM_000297.4:c.420G= MANE Select NP_000288.1:p.Gly140=
NR_156488.2:n.519G=