Canonical Allele Identifier: CA357626698
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008184A>T , CM000666.2:g.88008184A>T GRCh38
NC_000004.11:g.88929336A>T , CM000666.1:g.88929336A>T GRCh37
NC_000004.10:g.89148360A>T NCBI36
NG_008604.1:g.5517A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.451A>T MANE Select ENSP00000237596.2:p.Ser151Cys
ENST00000237596.6:c.451A>T ENSP00000237596.2:p.Ser151Cys
NM_000297.3:c.451A>T NP_000288.1:p.Ser151Cys
XM_011532028.1:c.451A>T XP_011530330.1:p.Ser151Cys
XR_244632.2:n.546A>T
NR_156488.1:n.538A>T
XM_011532028.2:c.451A>T XP_011530330.1:p.Ser151Cys
NM_000297.4:c.451A>T MANE Select NP_000288.1:p.Ser151Cys
NR_156488.2:n.550A>T