Canonical Allele Identifier: CA1474562475
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008354A= , CM000666.2:g.88008354A= GRCh38
NC_000004.11:g.88929506A= , CM000666.1:g.88929506A= GRCh37
NC_000004.10:g.89148530A= NCBI36
NG_008604.1:g.5687A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+26A= MANE Select ENSP00000237596.2:n.595+26A=
ENST00000237596.6:c.595+26A= ENSP00000237596.2:n.595+26A=
ENST00000506727.1:n.97+26A=
NM_000297.3:c.595+26A= NP_000288.1:n.595+26A=
XM_011532028.1:c.595+26A= XP_011530330.1:n.595+26A=
XR_244632.2:n.690+26A=
NR_156488.1:n.682+26A=
XM_011532028.2:c.595+26A= XP_011530330.1:n.595+26A=
NM_000297.4:c.595+26A= MANE Select NP_000288.1:n.595+26A=
NR_156488.2:n.694+26A=
Search 100 bp 5'
Search 100 bp 3'