Canonical Allele Identifier: CA1474562138
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007755C= , CM000666.2:g.88007755C= GRCh38
NC_000004.11:g.88928907C= , CM000666.1:g.88928907C= GRCh37
NC_000004.10:g.89147931C= NCBI36
NG_008604.1:g.5088C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.22C= MANE Select ENSP00000237596.2:p.Gln8=
ENST00000237596.6:c.22C= ENSP00000237596.2:p.Gln8=
NM_000297.3:c.22C= NP_000288.1:p.Gln8=
XM_011532028.1:c.22C= XP_011530330.1:p.Gln8=
XR_244632.2:n.117C=
NR_156488.1:n.109C=
XM_011532028.2:c.22C= XP_011530330.1:p.Gln8=
NM_000297.4:c.22C= MANE Select NP_000288.1:p.Gln8=
NR_156488.2:n.121C=