Canonical Allele Identifier: CA357627155
Gene: PKD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88929450T>A (hg19) chr4:g.88008298T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008298T>A , CM000666.2:g.88008298T>A GRCh38
NC_000004.11:g.88929450T>A , CM000666.1:g.88929450T>A GRCh37
NC_000004.10:g.89148474T>A NCBI36
NG_008604.1:g.5631T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.565T>A MANE Select ENSP00000237596.2:p.Trp189Arg
ENST00000237596.6:c.565T>A ENSP00000237596.2:p.Trp189Arg
ENST00000506727.1:n.67T>A
NM_000297.3:c.565T>A NP_000288.1:p.Trp189Arg
XM_011532028.1:c.565T>A XP_011530330.1:p.Trp189Arg
XR_244632.2:n.660T>A
NR_156488.1:n.652T>A
XM_011532028.2:c.565T>A XP_011530330.1:p.Trp189Arg
NM_000297.4:c.565T>A MANE Select NP_000288.1:p.Trp189Arg
NR_156488.2:n.664T>A
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