Canonical Allele Identifier: CA1474562149
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007772G= , CM000666.2:g.88007772G= GRCh38
NC_000004.11:g.88928924G= , CM000666.1:g.88928924G= GRCh37
NC_000004.10:g.89147948G= NCBI36
NG_008604.1:g.5105G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.39G= MANE Select ENSP00000237596.2:p.Gly13=
ENST00000237596.6:c.39G= ENSP00000237596.2:p.Gly13=
NM_000297.3:c.39G= NP_000288.1:p.Gly13=
XM_011532028.1:c.39G= XP_011530330.1:p.Gly13=
XR_244632.2:n.134G=
NR_156488.1:n.126G=
XM_011532028.2:c.39G= XP_011530330.1:p.Gly13=
NM_000297.4:c.39G= MANE Select NP_000288.1:p.Gly13=
NR_156488.2:n.138G=