Canonical Allele Identifier: CA1474562029
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1235606078
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007641C>G , CM000666.2:g.88007641C>G GRCh38
NC_000004.11:g.88928793C>G , CM000666.1:g.88928793C>G GRCh37
NC_000004.10:g.89147817C>G NCBI36
NG_008604.1:g.4974C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-93C>G MANE Select ENSP00000237596.2:n.-93C>G
XR_244632.2:n.3C>G
NM_000297.4:c.-93C>G MANE Select NP_000288.1:n.-93C>G
NR_156488.2:n.7C>G
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