Canonical Allele Identifier: CA357626984
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008254-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008254T>C , CM000666.2:g.88008254T>C GRCh38
NC_000004.11:g.88929406T>C , CM000666.1:g.88929406T>C GRCh37
NC_000004.10:g.89148430T>C NCBI36
NG_008604.1:g.5587T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.521T>C MANE Select ENSP00000237596.2:p.Leu174Pro
ENST00000237596.6:c.521T>C ENSP00000237596.2:p.Leu174Pro
ENST00000506727.1:n.23T>C
NM_000297.3:c.521T>C NP_000288.1:p.Leu174Pro
XM_011532028.1:c.521T>C XP_011530330.1:p.Leu174Pro
XR_244632.2:n.616T>C
NR_156488.1:n.608T>C
XM_011532028.2:c.521T>C XP_011530330.1:p.Leu174Pro
NM_000297.4:c.521T>C MANE Select NP_000288.1:p.Leu174Pro
NR_156488.2:n.620T>C