Canonical Allele Identifier: CA1474562583
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1726275566

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008537T>A , CM000666.2:g.88008537T>A GRCh38
NC_000004.11:g.88929689T>A , CM000666.1:g.88929689T>A GRCh37
NC_000004.10:g.89148713T>A NCBI36
NG_008604.1:g.5870T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+209T>A MANE Select ENSP00000237596.2:n.595+209T>A
ENST00000237596.6:c.595+209T>A ENSP00000237596.2:n.595+209T>A
ENST00000506727.1:n.97+209T>A
NM_000297.3:c.595+209T>A NP_000288.1:n.595+209T>A
XM_011532028.1:c.595+209T>A XP_011530330.1:n.595+209T>A
XR_244632.2:n.690+209T>A
NR_156488.1:n.682+209T>A
XM_011532028.2:c.595+209T>A XP_011530330.1:n.595+209T>A
NM_000297.4:c.595+209T>A MANE Select NP_000288.1:n.595+209T>A
NR_156488.2:n.694+209T>A