Canonical Allele Identifier: CA440297105
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008255-G-T
MyVariant Identifiers: chr4:g.88929407G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008255G>T , CM000666.2:g.88008255G>T GRCh38
NC_000004.11:g.88929407G>T , CM000666.1:g.88929407G>T GRCh37
NC_000004.10:g.89148431G>T NCBI36
NG_008604.1:g.5588G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.522G>T MANE Select ENSP00000237596.2:p.Leu174=
ENST00000237596.6:c.522G>T ENSP00000237596.2:p.Leu174=
ENST00000506727.1:n.24G>T
NM_000297.3:c.522G>T NP_000288.1:p.Leu174=
XM_011532028.1:c.522G>T XP_011530330.1:p.Leu174=
XR_244632.2:n.617G>T
NR_156488.1:n.609G>T
XM_011532028.2:c.522G>T XP_011530330.1:p.Leu174=
NM_000297.4:c.522G>T MANE Select NP_000288.1:p.Leu174=
NR_156488.2:n.621G>T