Canonical Allele Identifier: CA1474562051
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007668G= , CM000666.2:g.88007668G= GRCh38
NC_000004.11:g.88928820G= , CM000666.1:g.88928820G= GRCh37
NC_000004.10:g.89147844G= NCBI36
NG_008604.1:g.5001G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-66G= MANE Select ENSP00000237596.2:n.-66G=
ENST00000237596.6:c.-66G= ENSP00000237596.2:n.-66G=
NM_000297.3:c.-66G= NP_000288.1:n.-66G=
XM_011532028.1:c.-66G= XP_011530330.1:n.-66G=
XR_244632.2:n.30G=
NR_156488.1:n.22G=
XM_011532028.2:c.-66G= XP_011530330.1:n.-66G=
NM_000297.4:c.-66G= MANE Select NP_000288.1:n.-66G=
NR_156488.2:n.34G=
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