Canonical Allele Identifier: CA440296857
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008135-G-T
MyVariant Identifiers: chr4:g.88929287G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008135G>T , CM000666.2:g.88008135G>T GRCh38
NC_000004.11:g.88929287G>T , CM000666.1:g.88929287G>T GRCh37
NC_000004.10:g.89148311G>T NCBI36
NG_008604.1:g.5468G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.402G>T MANE Select ENSP00000237596.2:p.Val134=
ENST00000237596.6:c.402G>T ENSP00000237596.2:p.Val134=
NM_000297.3:c.402G>T NP_000288.1:p.Val134=
XM_011532028.1:c.402G>T XP_011530330.1:p.Val134=
XR_244632.2:n.497G>T
NR_156488.1:n.489G>T
XM_011532028.2:c.402G>T XP_011530330.1:p.Val134=
NM_000297.4:c.402G>T MANE Select NP_000288.1:p.Val134=
NR_156488.2:n.501G>T