Canonical Allele Identifier: CA1474562037
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007651C= , CM000666.2:g.88007651C= GRCh38
NC_000004.11:g.88928803C= , CM000666.1:g.88928803C= GRCh37
NC_000004.10:g.89147827C= NCBI36
NG_008604.1:g.4984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-83C= MANE Select ENSP00000237596.2:n.-83C=
NM_000297.3:c.-83C= NP_000288.1:n.-83C=
XM_011532028.1:c.-83C= XP_011530330.1:n.-83C=
XR_244632.2:n.13C=
NR_156488.1:n.5C=
NM_000297.4:c.-83C= MANE Select NP_000288.1:n.-83C=
NR_156488.2:n.17C=