Canonical Allele Identifier: CA1474562415
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008264C= , CM000666.2:g.88008264C= GRCh38
NC_000004.11:g.88929416C= , CM000666.1:g.88929416C= GRCh37
NC_000004.10:g.89148440C= NCBI36
NG_008604.1:g.5597C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.531C= MANE Select ENSP00000237596.2:p.His177=
ENST00000237596.6:c.531C= ENSP00000237596.2:p.His177=
ENST00000506727.1:n.33C=
NM_000297.3:c.531C= NP_000288.1:p.His177=
XM_011532028.1:c.531C= XP_011530330.1:p.His177=
XR_244632.2:n.626C=
NR_156488.1:n.618C=
XM_011532028.2:c.531C= XP_011530330.1:p.His177=
NM_000297.4:c.531C= MANE Select NP_000288.1:p.His177=
NR_156488.2:n.630C=