Canonical Allele Identifier: CA799592380
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1347185573
gnomAD v3: 4-88007635-A-AGGC
gnomAD v4: 4-88007635-A-AGGC
MyVariant Identifiers: chr4:g.88928787_88928788insGGC (hg19) chr4:g.88007635_88007636insGGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007644_88007646dup , CM000666.2:g.88007644_88007646dup GRCh38
NC_000004.11:g.88928796_88928798dup , CM000666.1:g.88928796_88928798dup GRCh37
NC_000004.10:g.89147820_89147822dup NCBI36
NG_008604.1:g.4977_4979dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-90_-88dup MANE Select ENSP00000237596.2:n.-90_-88dup
NM_000297.4:c.-90_-88dup MANE Select NP_000288.1:n.-90_-88dup
NR_156488.2:n.10_12dup
Search 100 bp 5'
Search 100 bp 3'