Canonical Allele Identifier: CA1474562032
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007643G= , CM000666.2:g.88007643G= GRCh38
NC_000004.11:g.88928795G= , CM000666.1:g.88928795G= GRCh37
NC_000004.10:g.89147819G= NCBI36
NG_008604.1:g.4976G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-91G= MANE Select ENSP00000237596.2:n.-91G=
XR_244632.2:n.5G=
NM_000297.4:c.-91G= MANE Select NP_000288.1:n.-91G=
NR_156488.2:n.9G=
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