Canonical Allele Identifier: CA1474562387
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008197G= , CM000666.2:g.88008197G= GRCh38
NC_000004.11:g.88929349G= , CM000666.1:g.88929349G= GRCh37
NC_000004.10:g.89148373G= NCBI36
NG_008604.1:g.5530G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.464G= MANE Select ENSP00000237596.2:p.Arg155=
ENST00000237596.6:c.464G= ENSP00000237596.2:p.Arg155=
NM_000297.3:c.464G= NP_000288.1:p.Arg155=
XM_011532028.1:c.464G= XP_011530330.1:p.Arg155=
XR_244632.2:n.559G=
NR_156488.1:n.551G=
XM_011532028.2:c.464G= XP_011530330.1:p.Arg155=
NM_000297.4:c.464G= MANE Select NP_000288.1:p.Arg155=
NR_156488.2:n.563G=