Canonical Allele Identifier: CA2671365065
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs2110079898
gnomAD v4: 4-88007676-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007676A>G , CM000666.2:g.88007676A>G GRCh38
NC_000004.11:g.88928828A>G , CM000666.1:g.88928828A>G GRCh37
NC_000004.10:g.89147852A>G NCBI36
NG_008604.1:g.5009A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-58A>G MANE Select ENSP00000237596.2:n.-58A>G
ENST00000237596.6:c.-58A>G ENSP00000237596.2:n.-58A>G
NM_000297.3:c.-58A>G NP_000288.1:n.-58A>G
XM_011532028.1:c.-58A>G XP_011530330.1:n.-58A>G
XR_244632.2:n.38A>G
NR_156488.1:n.30A>G
XM_011532028.2:c.-58A>G XP_011530330.1:n.-58A>G
NM_000297.4:c.-58A>G MANE Select NP_000288.1:n.-58A>G
NR_156488.2:n.42A>G
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