Canonical Allele Identifier: CA1474562279
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007989G= , CM000666.2:g.88007989G= GRCh38
NC_000004.11:g.88929141G= , CM000666.1:g.88929141G= GRCh37
NC_000004.10:g.89148165G= NCBI36
NG_008604.1:g.5322G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.256G= MANE Select ENSP00000237596.2:p.Ala86=
ENST00000237596.6:c.256G= ENSP00000237596.2:p.Ala86=
NM_000297.3:c.256G= NP_000288.1:p.Ala86=
XM_011532028.1:c.256G= XP_011530330.1:p.Ala86=
XR_244632.2:n.351G=
NR_156488.1:n.343G=
XM_011532028.2:c.256G= XP_011530330.1:p.Ala86=
NM_000297.4:c.256G= MANE Select NP_000288.1:p.Ala86=
NR_156488.2:n.355G=