Canonical Allele Identifier: CA1474562096
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007707C= , CM000666.2:g.88007707C= GRCh38
NC_000004.11:g.88928859C= , CM000666.1:g.88928859C= GRCh37
NC_000004.10:g.89147883C= NCBI36
NG_008604.1:g.5040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-27C= MANE Select ENSP00000237596.2:n.-27C=
ENST00000237596.6:c.-27C= ENSP00000237596.2:n.-27C=
NM_000297.3:c.-27C= NP_000288.1:n.-27C=
XM_011532028.1:c.-27C= XP_011530330.1:n.-27C=
XR_244632.2:n.69C=
NR_156488.1:n.61C=
XM_011532028.2:c.-27C= XP_011530330.1:n.-27C=
NM_000297.4:c.-27C= MANE Select NP_000288.1:n.-27C=
NR_156488.2:n.73C=
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