Canonical Allele Identifier: CA1474562035
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007646G= , CM000666.2:g.88007646G= GRCh38
NC_000004.11:g.88928798G= , CM000666.1:g.88928798G= GRCh37
NC_000004.10:g.89147822G= NCBI36
NG_008604.1:g.4979G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-88G= MANE Select ENSP00000237596.2:n.-88G=
XM_011532028.1:c.-88G= XP_011530330.1:n.-88G=
XR_244632.2:n.8G=
NM_000297.4:c.-88G= MANE Select NP_000288.1:n.-88G=
NR_156488.2:n.12G=
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