Canonical Allele Identifier: CA357626542
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs2110080507

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008145A>G , CM000666.2:g.88008145A>G GRCh38
NC_000004.11:g.88929297A>G , CM000666.1:g.88929297A>G GRCh37
NC_000004.10:g.89148321A>G NCBI36
NG_008604.1:g.5478A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.412A>G MANE Select ENSP00000237596.2:p.Ser138Gly
ENST00000237596.6:c.412A>G ENSP00000237596.2:p.Ser138Gly
NM_000297.3:c.412A>G NP_000288.1:p.Ser138Gly
XM_011532028.1:c.412A>G XP_011530330.1:p.Ser138Gly
XR_244632.2:n.507A>G
NR_156488.1:n.499A>G
XM_011532028.2:c.412A>G XP_011530330.1:p.Ser138Gly
NM_000297.4:c.412A>G MANE Select NP_000288.1:p.Ser138Gly
NR_156488.2:n.511A>G