Canonical Allele Identifier: CA357626374
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008095-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008095G>T , CM000666.2:g.88008095G>T GRCh38
NC_000004.11:g.88929247G>T , CM000666.1:g.88929247G>T GRCh37
NC_000004.10:g.89148271G>T NCBI36
NG_008604.1:g.5428G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.362G>T MANE Select ENSP00000237596.2:p.Gly121Val
ENST00000237596.6:c.362G>T ENSP00000237596.2:p.Gly121Val
NM_000297.3:c.362G>T NP_000288.1:p.Gly121Val
XM_011532028.1:c.362G>T XP_011530330.1:p.Gly121Val
XR_244632.2:n.457G>T
NR_156488.1:n.449G>T
XM_011532028.2:c.362G>T XP_011530330.1:p.Gly121Val
NM_000297.4:c.362G>T MANE Select NP_000288.1:p.Gly121Val
NR_156488.2:n.461G>T