Canonical Allele Identifier: CA357626029
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008020C>G , CM000666.2:g.88008020C>G GRCh38
NC_000004.11:g.88929172C>G , CM000666.1:g.88929172C>G GRCh37
NC_000004.10:g.89148196C>G NCBI36
NG_008604.1:g.5353C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.287C>G MANE Select ENSP00000237596.2:p.Ala96Gly
ENST00000237596.6:c.287C>G ENSP00000237596.2:p.Ala96Gly
NM_000297.3:c.287C>G NP_000288.1:p.Ala96Gly
XM_011532028.1:c.287C>G XP_011530330.1:p.Ala96Gly
XR_244632.2:n.382C>G
NR_156488.1:n.374C>G
XM_011532028.2:c.287C>G XP_011530330.1:p.Ala96Gly
NM_000297.4:c.287C>G MANE Select NP_000288.1:p.Ala96Gly
NR_156488.2:n.386C>G