Canonical Allele Identifier: CA357625248
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007848A>T , CM000666.2:g.88007848A>T GRCh38
NC_000004.11:g.88929000A>T , CM000666.1:g.88929000A>T GRCh37
NC_000004.10:g.89148024A>T NCBI36
NG_008604.1:g.5181A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.115A>T MANE Select ENSP00000237596.2:p.Ser39Cys
ENST00000237596.6:c.115A>T ENSP00000237596.2:p.Ser39Cys
NM_000297.3:c.115A>T NP_000288.1:p.Ser39Cys
XM_011532028.1:c.115A>T XP_011530330.1:p.Ser39Cys
XR_244632.2:n.210A>T
NR_156488.1:n.202A>T
XM_011532028.2:c.115A>T XP_011530330.1:p.Ser39Cys
NM_000297.4:c.115A>T MANE Select NP_000288.1:p.Ser39Cys
NR_156488.2:n.214A>T