Canonical Allele Identifier: CA1474562423
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008278G= , CM000666.2:g.88008278G= GRCh38
NC_000004.11:g.88929430G= , CM000666.1:g.88929430G= GRCh37
NC_000004.10:g.89148454G= NCBI36
NG_008604.1:g.5611G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.545G= MANE Select ENSP00000237596.2:p.Gly182=
ENST00000237596.6:c.545G= ENSP00000237596.2:p.Gly182=
ENST00000506727.1:n.47G=
NM_000297.3:c.545G= NP_000288.1:p.Gly182=
XM_011532028.1:c.545G= XP_011530330.1:p.Gly182=
XR_244632.2:n.640G=
NR_156488.1:n.632G=
XM_011532028.2:c.545G= XP_011530330.1:p.Gly182=
NM_000297.4:c.545G= MANE Select NP_000288.1:p.Gly182=
NR_156488.2:n.644G=