Canonical Allele Identifier: CA1474562039
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007652G= , CM000666.2:g.88007652G= GRCh38
NC_000004.11:g.88928804G= , CM000666.1:g.88928804G= GRCh37
NC_000004.10:g.89147828G= NCBI36
NG_008604.1:g.4985G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-82G= MANE Select ENSP00000237596.2:n.-82G=
NM_000297.3:c.-82G= NP_000288.1:n.-82G=
XM_011532028.1:c.-82G= XP_011530330.1:n.-82G=
XR_244632.2:n.14G=
NR_156488.1:n.6G=
NM_000297.4:c.-82G= MANE Select NP_000288.1:n.-82G=
NR_156488.2:n.18G=