Canonical Allele Identifier: CA799592512
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1271648585
gnomAD v3: 4-88007726-T-C
gnomAD v4: 4-88007726-T-C
MyVariant Identifiers: chr4:g.88928878T>C (hg19) chr4:g.88007726T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007726T>C , CM000666.2:g.88007726T>C GRCh38
NC_000004.11:g.88928878T>C , CM000666.1:g.88928878T>C GRCh37
NC_000004.10:g.89147902T>C NCBI36
NG_008604.1:g.5059T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-8T>C MANE Select ENSP00000237596.2:n.-8T>C
ENST00000237596.6:c.-8T>C ENSP00000237596.2:n.-8T>C
NM_000297.3:c.-8T>C NP_000288.1:n.-8T>C
XM_011532028.1:c.-8T>C XP_011530330.1:n.-8T>C
XR_244632.2:n.88T>C
NR_156488.1:n.80T>C
XM_011532028.2:c.-8T>C XP_011530330.1:n.-8T>C
NM_000297.4:c.-8T>C MANE Select NP_000288.1:n.-8T>C
NR_156488.2:n.92T>C
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