Canonical Allele Identifier: CA357624776
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007741-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007741A>G , CM000666.2:g.88007741A>G GRCh38
NC_000004.11:g.88928893A>G , CM000666.1:g.88928893A>G GRCh37
NC_000004.10:g.89147917A>G NCBI36
NG_008604.1:g.5074A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.8A>G MANE Select ENSP00000237596.2:p.Asn3Ser
ENST00000237596.6:c.8A>G ENSP00000237596.2:p.Asn3Ser
NM_000297.3:c.8A>G NP_000288.1:p.Asn3Ser
XM_011532028.1:c.8A>G XP_011530330.1:p.Asn3Ser
XR_244632.2:n.103A>G
NR_156488.1:n.95A>G
XM_011532028.2:c.8A>G XP_011530330.1:p.Asn3Ser
NM_000297.4:c.8A>G MANE Select NP_000288.1:p.Asn3Ser
NR_156488.2:n.107A>G