Canonical Allele Identifier: CA357626997
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.524A>C MANE Select ENSP00000237596.2:p.His175Pro
ENST00000237596.6:c.524A>C ENSP00000237596.2:p.His175Pro
ENST00000506727.1:n.26A>C
NM_000297.3:c.524A>C NP_000288.1:p.His175Pro
XM_011532028.1:c.524A>C XP_011530330.1:p.His175Pro
XR_244632.2:n.619A>C
NR_156488.1:n.611A>C
XM_011532028.2:c.524A>C XP_011530330.1:p.His175Pro
NM_000297.4:c.524A>C MANE Select NP_000288.1:p.His175Pro
NR_156488.2:n.623A>C