Canonical Allele Identifier: CA357624857
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007765-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007765A>G , CM000666.2:g.88007765A>G GRCh38
NC_000004.11:g.88928917A>G , CM000666.1:g.88928917A>G GRCh37
NC_000004.10:g.89147941A>G NCBI36
NG_008604.1:g.5098A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.32A>G MANE Select ENSP00000237596.2:p.Gln11Arg
ENST00000237596.6:c.32A>G ENSP00000237596.2:p.Gln11Arg
NM_000297.3:c.32A>G NP_000288.1:p.Gln11Arg
XM_011532028.1:c.32A>G XP_011530330.1:p.Gln11Arg
XR_244632.2:n.127A>G
NR_156488.1:n.119A>G
XM_011532028.2:c.32A>G XP_011530330.1:p.Gln11Arg
NM_000297.4:c.32A>G MANE Select NP_000288.1:p.Gln11Arg
NR_156488.2:n.131A>G