Canonical Allele Identifier: CA1474562571
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1726274756
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008507G>A , CM000666.2:g.88008507G>A GRCh38
NC_000004.11:g.88929659G>A , CM000666.1:g.88929659G>A GRCh37
NC_000004.10:g.89148683G>A NCBI36
NG_008604.1:g.5840G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+179G>A MANE Select ENSP00000237596.2:n.595+179G>A
ENST00000237596.6:c.595+179G>A ENSP00000237596.2:n.595+179G>A
ENST00000506727.1:n.97+179G>A
NM_000297.3:c.595+179G>A NP_000288.1:n.595+179G>A
XM_011532028.1:c.595+179G>A XP_011530330.1:n.595+179G>A
XR_244632.2:n.690+179G>A
NR_156488.1:n.682+179G>A
XM_011532028.2:c.595+179G>A XP_011530330.1:n.595+179G>A
NM_000297.4:c.595+179G>A MANE Select NP_000288.1:n.595+179G>A
NR_156488.2:n.694+179G>A
Search 100 bp 5'
Search 100 bp 3'