Canonical Allele Identifier: CA357626847
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1434116020
gnomAD v4: 4-88008220-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008220C>T , CM000666.2:g.88008220C>T GRCh38
NC_000004.11:g.88929372C>T , CM000666.1:g.88929372C>T GRCh37
NC_000004.10:g.89148396C>T NCBI36
NG_008604.1:g.5553C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.487C>T MANE Select ENSP00000237596.2:p.Pro163Ser
ENST00000237596.6:c.487C>T ENSP00000237596.2:p.Pro163Ser
NM_000297.3:c.487C>T NP_000288.1:p.Pro163Ser
XM_011532028.1:c.487C>T XP_011530330.1:p.Pro163Ser
XR_244632.2:n.582C>T
NR_156488.1:n.574C>T
XM_011532028.2:c.487C>T XP_011530330.1:p.Pro163Ser
NM_000297.4:c.487C>T MANE Select NP_000288.1:p.Pro163Ser
NR_156488.2:n.586C>T