Canonical Allele Identifier: CA10621930

Gene: PKD2

Linked Data

• ClinVar Variation Id: 350027
• ClinVar RCV Id: RCV000405768 ; RCV001421071
• dbSNP Id: rs886059702
• gnomAD v2: 4-88986905-T-C
• gnomAD v3: 4-88065753-T-C
• gnomAD v4: 4-88065753-T-C
• MyVariant Identifiers: chr4:g.88986905T>C (hg19) ; chr4:g.88065753T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88065753T>C , CM000666.2:g.88065753T>C	GRCh38
NC_000004.11:g.88986905T>C , CM000666.1:g.88986905T>C	GRCh37
NC_000004.10:g.89205929T>C	NCBI36
NG_008604.1:g.63086T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.2241-9T>C MANE Select	ENSP00000237596.2:n.2241-9T>C
ENST00000237596.6:c.2241-9T>C	ENSP00000237596.2:n.2241-9T>C
ENST00000502363.1:c.495-9T>C	ENSP00000425289.1:n.495-9T>C
ENST00000508588.5:c.495-9T>C	ENSP00000427131.1:n.495-9T>C
ENST00000511337.5:n.493-9T>C
ENST00000512858.1:n.710T>C
NM_000297.3:c.2241-9T>C	NP_000288.1:n.2241-9T>C
XM_011532028.1:c.2016-9T>C	XP_011530330.1:n.2016-9T>C
XM_011532029.1:c.1521-9T>C	XP_011530331.1:n.1521-9T>C
XM_011532030.1:c.1401-9T>C	XP_011530332.1:n.1401-9T>C
NR_156488.1:n.2207-9T>C
XM_011532028.2:c.2016-9T>C	XP_011530330.1:n.2016-9T>C
XM_011532030.2:c.1401-9T>C	XP_011530332.1:n.1401-9T>C
NM_000297.4:c.2241-9T>C MANE Select	NP_000288.1:n.2241-9T>C
NR_156488.2:n.2219-9T>C