Canonical Allele Identifier: CA1474562047
Gene: PKD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007664A= , CM000666.2:g.88007664A= GRCh38
NC_000004.11:g.88928816A= , CM000666.1:g.88928816A= GRCh37
NC_000004.10:g.89147840A= NCBI36
NG_008604.1:g.4997A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-70A= MANE Select ENSP00000237596.2:n.-70A=
NM_000297.3:c.-70A= NP_000288.1:n.-70A=
XM_011532028.1:c.-70A= XP_011530330.1:n.-70A=
XR_244632.2:n.26A=
NR_156488.1:n.18A=
XM_011532028.2:c.-70A= XP_011530330.1:n.-70A=
NM_000297.4:c.-70A= MANE Select NP_000288.1:n.-70A=
NR_156488.2:n.30A=
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