Canonical Allele Identifier: CA357626999
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008257A>G , CM000666.2:g.88008257A>G GRCh38
NC_000004.11:g.88929409A>G , CM000666.1:g.88929409A>G GRCh37
NC_000004.10:g.89148433A>G NCBI36
NG_008604.1:g.5590A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.524A>G MANE Select ENSP00000237596.2:p.His175Arg
ENST00000237596.6:c.524A>G ENSP00000237596.2:p.His175Arg
ENST00000506727.1:n.26A>G
NM_000297.3:c.524A>G NP_000288.1:p.His175Arg
XM_011532028.1:c.524A>G XP_011530330.1:p.His175Arg
XR_244632.2:n.619A>G
NR_156488.1:n.611A>G
XM_011532028.2:c.524A>G XP_011530330.1:p.His175Arg
NM_000297.4:c.524A>G MANE Select NP_000288.1:p.His175Arg
NR_156488.2:n.623A>G