Canonical Allele Identifier: CA357624748
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007735-T-C
MyVariant Identifiers: chr4:g.88928887T>C (hg19) chr4:g.88007735T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007735T>C , CM000666.2:g.88007735T>C GRCh38
NC_000004.11:g.88928887T>C , CM000666.1:g.88928887T>C GRCh37
NC_000004.10:g.89147911T>C NCBI36
NG_008604.1:g.5068T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.2T>C MANE Select ENSP00000237596.2:p.Met1Thr
ENST00000237596.6:c.2T>C ENSP00000237596.2:p.Met1Thr
NM_000297.3:c.2T>C NP_000288.1:p.Met1Thr
XM_011532028.1:c.2T>C XP_011530330.1:p.Met1Thr
XR_244632.2:n.97T>C
NR_156488.1:n.89T>C
XM_011532028.2:c.2T>C XP_011530330.1:p.Met1Thr
NM_000297.4:c.2T>C MANE Select NP_000288.1:p.Met1Thr
NR_156488.2:n.101T>C
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