Canonical Allele Identifier: CA1474562513
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1726269524

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008410T>G , CM000666.2:g.88008410T>G GRCh38
NC_000004.11:g.88929562T>G , CM000666.1:g.88929562T>G GRCh37
NC_000004.10:g.89148586T>G NCBI36
NG_008604.1:g.5743T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.595+82T>G MANE Select ENSP00000237596.2:n.595+82T>G
ENST00000237596.6:c.595+82T>G ENSP00000237596.2:n.595+82T>G
ENST00000506727.1:n.97+82T>G
NM_000297.3:c.595+82T>G NP_000288.1:n.595+82T>G
XM_011532028.1:c.595+82T>G XP_011530330.1:n.595+82T>G
XR_244632.2:n.690+82T>G
NR_156488.1:n.682+82T>G
XM_011532028.2:c.595+82T>G XP_011530330.1:n.595+82T>G
NM_000297.4:c.595+82T>G MANE Select NP_000288.1:n.595+82T>G
NR_156488.2:n.694+82T>G