Canonical Allele Identifier: CA440268289
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007745-C-G
MyVariant Identifiers: chr4:g.88928897C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007745C>G , CM000666.2:g.88007745C>G GRCh38
NC_000004.11:g.88928897C>G , CM000666.1:g.88928897C>G GRCh37
NC_000004.10:g.89147921C>G NCBI36
NG_008604.1:g.5078C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.12C>G MANE Select ENSP00000237596.2:p.Ser4=
ENST00000237596.6:c.12C>G ENSP00000237596.2:p.Ser4=
NM_000297.3:c.12C>G NP_000288.1:p.Ser4=
XM_011532028.1:c.12C>G XP_011530330.1:p.Ser4=
XR_244632.2:n.107C>G
NR_156488.1:n.99C>G
XM_011532028.2:c.12C>G XP_011530330.1:p.Ser4=
NM_000297.4:c.12C>G MANE Select NP_000288.1:p.Ser4=
NR_156488.2:n.111C>G
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