Canonical Allele Identifier: CA357624898
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007774-A-G
MyVariant Identifiers: chr4:g.88928926A>G (hg19) chr4:g.88007774A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007774A>G , CM000666.2:g.88007774A>G GRCh38
NC_000004.11:g.88928926A>G , CM000666.1:g.88928926A>G GRCh37
NC_000004.10:g.89147950A>G NCBI36
NG_008604.1:g.5107A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.41A>G MANE Select ENSP00000237596.2:p.Asp14Gly
ENST00000237596.6:c.41A>G ENSP00000237596.2:p.Asp14Gly
NM_000297.3:c.41A>G NP_000288.1:p.Asp14Gly
XM_011532028.1:c.41A>G XP_011530330.1:p.Asp14Gly
XR_244632.2:n.136A>G
NR_156488.1:n.128A>G
XM_011532028.2:c.41A>G XP_011530330.1:p.Asp14Gly
NM_000297.4:c.41A>G MANE Select NP_000288.1:p.Asp14Gly
NR_156488.2:n.140A>G
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