Canonical Allele Identifier: CA2762537017
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008347C>G , CM000666.2:g.88008347C>G GRCh38
NC_000004.11:g.88929499C>G , CM000666.1:g.88929499C>G GRCh37
NC_000004.10:g.89148523C>G NCBI36
NG_008604.1:g.5680C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+19C>G MANE Select ENSP00000237596.2:n.595+19C>G
ENST00000237596.6:c.595+19C>G ENSP00000237596.2:n.595+19C>G
ENST00000506727.1:n.97+19C>G
NM_000297.3:c.595+19C>G NP_000288.1:n.595+19C>G
XM_011532028.1:c.595+19C>G XP_011530330.1:n.595+19C>G
XR_244632.2:n.690+19C>G
NR_156488.1:n.682+19C>G
XM_011532028.2:c.595+19C>G XP_011530330.1:n.595+19C>G
NM_000297.4:c.595+19C>G MANE Select NP_000288.1:n.595+19C>G
NR_156488.2:n.694+19C>G