Canonical Allele Identifier: CA2671365784
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88038213-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038213G>T , CM000666.2:g.88038213G>T GRCh38
NC_000004.11:g.88959365G>T , CM000666.1:g.88959365G>T GRCh37
NC_000004.10:g.89178389G>T NCBI36
NG_008604.1:g.35546G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.844-38G>T MANE Select ENSP00000237596.2:n.844-38G>T
ENST00000237596.6:c.844-38G>T ENSP00000237596.2:n.844-38G>T
ENST00000506367.1:n.291-38G>T
ENST00000506727.1:n.430-38G>T
NM_000297.3:c.844-38G>T NP_000288.1:n.844-38G>T
XM_011532028.1:c.844-38G>T XP_011530330.1:n.844-38G>T
XM_011532029.1:c.124-38G>T XP_011530331.1:n.124-38G>T
XM_011532030.1:c.4-38G>T XP_011530332.1:n.4-38G>T
XR_244632.2:n.939-38G>T
NR_156488.1:n.931-38G>T
XM_011532028.2:c.844-38G>T XP_011530330.1:n.844-38G>T
XM_011532030.2:c.4-38G>T XP_011530332.1:n.4-38G>T
NM_000297.4:c.844-38G>T MANE Select NP_000288.1:n.844-38G>T
NR_156488.2:n.943-38G>T