Canonical Allele Identifier: CA1474562033
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1726212775
gnomAD v4: 4-88007643-G-A
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Genomic Alleles

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

Transcript Alleles

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