Canonical Allele Identifier: CA440297131
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1186707441
gnomAD v4: 4-88008270-C-A
MyVariant Identifiers: chr4:g.88929422C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008270C>A , CM000666.2:g.88008270C>A GRCh38
NC_000004.11:g.88929422C>A , CM000666.1:g.88929422C>A GRCh37
NC_000004.10:g.89148446C>A NCBI36
NG_008604.1:g.5603C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.537C>A MANE Select ENSP00000237596.2:p.Pro179=
ENST00000237596.6:c.537C>A ENSP00000237596.2:p.Pro179=
ENST00000506727.1:n.39C>A
NM_000297.3:c.537C>A NP_000288.1:p.Pro179=
XM_011532028.1:c.537C>A XP_011530330.1:p.Pro179=
XR_244632.2:n.632C>A
NR_156488.1:n.624C>A
XM_011532028.2:c.537C>A XP_011530330.1:p.Pro179=
NM_000297.4:c.537C>A MANE Select NP_000288.1:p.Pro179=
NR_156488.2:n.636C>A
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