Canonical Allele Identifier: CA3003729
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs775329795
gnomAD v2: 4-88929403-C-G
gnomAD v4: 4-88008251-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008251C>G , CM000666.2:g.88008251C>G GRCh38
NC_000004.11:g.88929403C>G , CM000666.1:g.88929403C>G GRCh37
NC_000004.10:g.89148427C>G NCBI36
NG_008604.1:g.5584C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.518C>G MANE Select ENSP00000237596.2:p.Pro173Arg
ENST00000237596.6:c.518C>G ENSP00000237596.2:p.Pro173Arg
ENST00000506727.1:n.20C>G
NM_000297.3:c.518C>G NP_000288.1:p.Pro173Arg
XM_011532028.1:c.518C>G XP_011530330.1:p.Pro173Arg
XR_244632.2:n.613C>G
NR_156488.1:n.605C>G
XM_011532028.2:c.518C>G XP_011530330.1:p.Pro173Arg
NM_000297.4:c.518C>G MANE Select NP_000288.1:p.Pro173Arg
NR_156488.2:n.617C>G