Canonical Allele Identifier: CA357625043
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1447102982
gnomAD v2: 4-88928962-C-A
gnomAD v4: 4-88007810-C-A
MyVariant Identifiers: chr4:g.88928962C>A (hg19) chr4:g.88007810C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007810C>A , CM000666.2:g.88007810C>A GRCh38
NC_000004.11:g.88928962C>A , CM000666.1:g.88928962C>A GRCh37
NC_000004.10:g.89147986C>A NCBI36
NG_008604.1:g.5143C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.77C>A MANE Select ENSP00000237596.2:p.Pro26Gln
ENST00000237596.6:c.77C>A ENSP00000237596.2:p.Pro26Gln
NM_000297.3:c.77C>A NP_000288.1:p.Pro26Gln
XM_011532028.1:c.77C>A XP_011530330.1:p.Pro26Gln
XR_244632.2:n.172C>A
NR_156488.1:n.164C>A
XM_011532028.2:c.77C>A XP_011530330.1:p.Pro26Gln
NM_000297.4:c.77C>A MANE Select NP_000288.1:p.Pro26Gln
NR_156488.2:n.176C>A
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