Canonical Allele Identifier: CA10621879
Gene: PKD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 350008
ClinVar RCV Id: RCV000290571
dbSNP Id: rs547865163
gnomAD v2: 4-88928818-A-G
gnomAD v3: 4-88007666-A-G
gnomAD v4: 4-88007666-A-G
MyVariant Identifiers: chr4:g.88928818A>G (hg19) chr4:g.88007666A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007666A>G , CM000666.2:g.88007666A>G GRCh38
NC_000004.11:g.88928818A>G , CM000666.1:g.88928818A>G GRCh37
NC_000004.10:g.89147842A>G NCBI36
NG_008604.1:g.4999A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-68A>G MANE Select ENSP00000237596.2:n.-68A>G
NM_000297.3:c.-68A>G NP_000288.1:n.-68A>G
XM_011532028.1:c.-68A>G XP_011530330.1:n.-68A>G
XR_244632.2:n.28A>G
NR_156488.1:n.20A>G
XM_011532028.2:c.-68A>G XP_011530330.1:n.-68A>G
NM_000297.4:c.-68A>G MANE Select NP_000288.1:n.-68A>G
NR_156488.2:n.32A>G
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