Canonical Allele Identifier: CA1474562403
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008229A= , CM000666.2:g.88008229A= GRCh38
NC_000004.11:g.88929381A= , CM000666.1:g.88929381A= GRCh37
NC_000004.10:g.89148405A= NCBI36
NG_008604.1:g.5562A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.496A= MANE Select ENSP00000237596.2:p.Ser166=
ENST00000237596.6:c.496A= ENSP00000237596.2:p.Ser166=
NM_000297.3:c.496A= NP_000288.1:p.Ser166=
XM_011532028.1:c.496A= XP_011530330.1:p.Ser166=
XR_244632.2:n.591A=
NR_156488.1:n.583A=
XM_011532028.2:c.496A= XP_011530330.1:p.Ser166=
NM_000297.4:c.496A= MANE Select NP_000288.1:p.Ser166=
NR_156488.2:n.595A=