Canonical Allele Identifier: CA2762537020
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008364A>G , CM000666.2:g.88008364A>G GRCh38
NC_000004.11:g.88929516A>G , CM000666.1:g.88929516A>G GRCh37
NC_000004.10:g.89148540A>G NCBI36
NG_008604.1:g.5697A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+36A>G MANE Select ENSP00000237596.2:n.595+36A>G
ENST00000237596.6:c.595+36A>G ENSP00000237596.2:n.595+36A>G
ENST00000506727.1:n.97+36A>G
NM_000297.3:c.595+36A>G NP_000288.1:n.595+36A>G
XM_011532028.1:c.595+36A>G XP_011530330.1:n.595+36A>G
XR_244632.2:n.690+36A>G
NR_156488.1:n.682+36A>G
XM_011532028.2:c.595+36A>G XP_011530330.1:n.595+36A>G
NM_000297.4:c.595+36A>G MANE Select NP_000288.1:n.595+36A>G
NR_156488.2:n.694+36A>G