Canonical Allele Identifier: CA440296749
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1329695809
gnomAD v3: 4-88008033-G-A
gnomAD v4: 4-88008033-G-A
MyVariant Identifiers: chr4:g.88929185G>A (hg19) chr4:g.88008033G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008033G>A , CM000666.2:g.88008033G>A GRCh38
NC_000004.11:g.88929185G>A , CM000666.1:g.88929185G>A GRCh37
NC_000004.10:g.89148209G>A NCBI36
NG_008604.1:g.5366G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.300G>A MANE Select ENSP00000237596.2:p.Glu100=
ENST00000237596.6:c.300G>A ENSP00000237596.2:p.Glu100=
NM_000297.3:c.300G>A NP_000288.1:p.Glu100=
XM_011532028.1:c.300G>A XP_011530330.1:p.Glu100=
XR_244632.2:n.395G>A
NR_156488.1:n.387G>A
XM_011532028.2:c.300G>A XP_011530330.1:p.Glu100=
NM_000297.4:c.300G>A MANE Select NP_000288.1:p.Glu100=
NR_156488.2:n.399G>A
Search 100 bp 5'
Search 100 bp 3'