Canonical Allele Identifier: CA1474562230
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007909T= , CM000666.2:g.88007909T= GRCh38
NC_000004.11:g.88929061T= , CM000666.1:g.88929061T= GRCh37
NC_000004.10:g.89148085T= NCBI36
NG_008604.1:g.5242T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.176T= MANE Select ENSP00000237596.2:p.Ile59=
ENST00000237596.6:c.176T= ENSP00000237596.2:p.Ile59=
NM_000297.3:c.176T= NP_000288.1:p.Ile59=
XM_011532028.1:c.176T= XP_011530330.1:p.Ile59=
XR_244632.2:n.271T=
NR_156488.1:n.263T=
XM_011532028.2:c.176T= XP_011530330.1:p.Ile59=
NM_000297.4:c.176T= MANE Select NP_000288.1:p.Ile59=
NR_156488.2:n.275T=