Canonical Allele Identifier: CA357626987
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008254T>G , CM000666.2:g.88008254T>G GRCh38
NC_000004.11:g.88929406T>G , CM000666.1:g.88929406T>G GRCh37
NC_000004.10:g.89148430T>G NCBI36
NG_008604.1:g.5587T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.521T>G MANE Select ENSP00000237596.2:p.Leu174Arg
ENST00000237596.6:c.521T>G ENSP00000237596.2:p.Leu174Arg
ENST00000506727.1:n.23T>G
NM_000297.3:c.521T>G NP_000288.1:p.Leu174Arg
XM_011532028.1:c.521T>G XP_011530330.1:p.Leu174Arg
XR_244632.2:n.616T>G
NR_156488.1:n.608T>G
XM_011532028.2:c.521T>G XP_011530330.1:p.Leu174Arg
NM_000297.4:c.521T>G MANE Select NP_000288.1:p.Leu174Arg
NR_156488.2:n.620T>G