Canonical Allele Identifier: CA440296511
Gene: PKD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88928996C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007844C>A , CM000666.2:g.88007844C>A GRCh38
NC_000004.11:g.88928996C>A , CM000666.1:g.88928996C>A GRCh37
NC_000004.10:g.89148020C>A NCBI36
NG_008604.1:g.5177C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.111C>A MANE Select ENSP00000237596.2:p.Gly37=
ENST00000237596.6:c.111C>A ENSP00000237596.2:p.Gly37=
NM_000297.3:c.111C>A NP_000288.1:p.Gly37=
XM_011532028.1:c.111C>A XP_011530330.1:p.Gly37=
XR_244632.2:n.206C>A
NR_156488.1:n.198C>A
XM_011532028.2:c.111C>A XP_011530330.1:p.Gly37=
NM_000297.4:c.111C>A MANE Select NP_000288.1:p.Gly37=
NR_156488.2:n.210C>A
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