Canonical Allele Identifier: CA357626970
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008250C>G , CM000666.2:g.88008250C>G GRCh38
NC_000004.11:g.88929402C>G , CM000666.1:g.88929402C>G GRCh37
NC_000004.10:g.89148426C>G NCBI36
NG_008604.1:g.5583C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.517C>G MANE Select ENSP00000237596.2:p.Pro173Ala
ENST00000237596.6:c.517C>G ENSP00000237596.2:p.Pro173Ala
ENST00000506727.1:n.19C>G
NM_000297.3:c.517C>G NP_000288.1:p.Pro173Ala
XM_011532028.1:c.517C>G XP_011530330.1:p.Pro173Ala
XR_244632.2:n.612C>G
NR_156488.1:n.604C>G
XM_011532028.2:c.517C>G XP_011530330.1:p.Pro173Ala
NM_000297.4:c.517C>G MANE Select NP_000288.1:p.Pro173Ala
NR_156488.2:n.616C>G