Canonical Allele Identifier: CA357626348
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008088C>G , CM000666.2:g.88008088C>G GRCh38
NC_000004.11:g.88929240C>G , CM000666.1:g.88929240C>G GRCh37
NC_000004.10:g.89148264C>G NCBI36
NG_008604.1:g.5421C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.355C>G MANE Select ENSP00000237596.2:p.Arg119Gly
ENST00000237596.6:c.355C>G ENSP00000237596.2:p.Arg119Gly
NM_000297.3:c.355C>G NP_000288.1:p.Arg119Gly
XM_011532028.1:c.355C>G XP_011530330.1:p.Arg119Gly
XR_244632.2:n.450C>G
NR_156488.1:n.442C>G
XM_011532028.2:c.355C>G XP_011530330.1:p.Arg119Gly
NM_000297.4:c.355C>G MANE Select NP_000288.1:p.Arg119Gly
NR_156488.2:n.454C>G