Canonical Allele Identifier: CA357626995
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008256-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008256C>T , CM000666.2:g.88008256C>T GRCh38
NC_000004.11:g.88929408C>T , CM000666.1:g.88929408C>T GRCh37
NC_000004.10:g.89148432C>T NCBI36
NG_008604.1:g.5589C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.523C>T MANE Select ENSP00000237596.2:p.His175Tyr
ENST00000237596.6:c.523C>T ENSP00000237596.2:p.His175Tyr
ENST00000506727.1:n.25C>T
NM_000297.3:c.523C>T NP_000288.1:p.His175Tyr
XM_011532028.1:c.523C>T XP_011530330.1:p.His175Tyr
XR_244632.2:n.618C>T
NR_156488.1:n.610C>T
XM_011532028.2:c.523C>T XP_011530330.1:p.His175Tyr
NM_000297.4:c.523C>T MANE Select NP_000288.1:p.His175Tyr
NR_156488.2:n.622C>T