Canonical Allele Identifier: CA1474562407
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008243C= , CM000666.2:g.88008243C= GRCh38
NC_000004.11:g.88929395C= , CM000666.1:g.88929395C= GRCh37
NC_000004.10:g.89148419C= NCBI36
NG_008604.1:g.5576C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.510C= MANE Select ENSP00000237596.2:p.Gly170=
ENST00000237596.6:c.510C= ENSP00000237596.2:p.Gly170=
ENST00000506727.1:n.12C=
NM_000297.3:c.510C= NP_000288.1:p.Gly170=
XM_011532028.1:c.510C= XP_011530330.1:p.Gly170=
XR_244632.2:n.605C=
NR_156488.1:n.597C=
XM_011532028.2:c.510C= XP_011530330.1:p.Gly170=
NM_000297.4:c.510C= MANE Select NP_000288.1:p.Gly170=
NR_156488.2:n.609C=