Canonical Allele Identifier: CA357626485
Gene: PKD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88929282T>A (hg19) chr4:g.88008130T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008130T>A , CM000666.2:g.88008130T>A GRCh38
NC_000004.11:g.88929282T>A , CM000666.1:g.88929282T>A GRCh37
NC_000004.10:g.89148306T>A NCBI36
NG_008604.1:g.5463T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.397T>A MANE Select ENSP00000237596.2:p.Ser133Thr
ENST00000237596.6:c.397T>A ENSP00000237596.2:p.Ser133Thr
NM_000297.3:c.397T>A NP_000288.1:p.Ser133Thr
XM_011532028.1:c.397T>A XP_011530330.1:p.Ser133Thr
XR_244632.2:n.492T>A
NR_156488.1:n.484T>A
XM_011532028.2:c.397T>A XP_011530330.1:p.Ser133Thr
NM_000297.4:c.397T>A MANE Select NP_000288.1:p.Ser133Thr
NR_156488.2:n.496T>A
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