Canonical Allele Identifier: CA1474562049
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007667T= , CM000666.2:g.88007667T= GRCh38
NC_000004.11:g.88928819T= , CM000666.1:g.88928819T= GRCh37
NC_000004.10:g.89147843T= NCBI36
NG_008604.1:g.5000T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-67T= MANE Select ENSP00000237596.2:n.-67T=
NM_000297.3:c.-67T= NP_000288.1:n.-67T=
XM_011532028.1:c.-67T= XP_011530330.1:n.-67T=
XR_244632.2:n.29T=
NR_156488.1:n.21T=
XM_011532028.2:c.-67T= XP_011530330.1:n.-67T=
NM_000297.4:c.-67T= MANE Select NP_000288.1:n.-67T=
NR_156488.2:n.33T=