Canonical Allele Identifier: CA2671365002
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007645-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007645G>A , CM000666.2:g.88007645G>A GRCh38
NC_000004.11:g.88928797G>A , CM000666.1:g.88928797G>A GRCh37
NC_000004.10:g.89147821G>A NCBI36
NG_008604.1:g.4978G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-89G>A MANE Select ENSP00000237596.2:n.-89G>A
XM_011532028.1:c.-89G>A XP_011530330.1:n.-89G>A
XR_244632.2:n.7G>A
NM_000297.4:c.-89G>A MANE Select NP_000288.1:n.-89G>A
NR_156488.2:n.11G>A