Canonical Allele Identifier: CA357624790
Gene: PKD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1810101
ClinVar RCV Id: RCV002508657
dbSNP Id: rs1726221678
gnomAD v4: 4-88007744-C-A
MyVariant Identifiers: chr4:g.88928896C>A (hg19) chr4:g.88007744C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007744C>A , CM000666.2:g.88007744C>A GRCh38
NC_000004.11:g.88928896C>A , CM000666.1:g.88928896C>A GRCh37
NC_000004.10:g.89147920C>A NCBI36
NG_008604.1:g.5077C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.11C>A MANE Select ENSP00000237596.2:p.Ser4Tyr
ENST00000237596.6:c.11C>A ENSP00000237596.2:p.Ser4Tyr
NM_000297.3:c.11C>A NP_000288.1:p.Ser4Tyr
XM_011532028.1:c.11C>A XP_011530330.1:p.Ser4Tyr
XR_244632.2:n.106C>A
NR_156488.1:n.98C>A
XM_011532028.2:c.11C>A XP_011530330.1:p.Ser4Tyr
NM_000297.4:c.11C>A MANE Select NP_000288.1:p.Ser4Tyr
NR_156488.2:n.110C>A
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