Canonical Allele Identifier: CA799594076

Gene: PKD2

Linked Data

• dbSNP Id: rs1202440520
• gnomAD v3: 4-88008541-T-C
• gnomAD v4: 4-88008541-T-C
• MyVariant Identifiers: chr4:g.88929693T>C (hg19) ; chr4:g.88008541T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88008541T>C , CM000666.2:g.88008541T>C	GRCh38
NC_000004.11:g.88929693T>C , CM000666.1:g.88929693T>C	GRCh37
NC_000004.10:g.89148717T>C	NCBI36
NG_008604.1:g.5874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.595+213T>C MANE Select	ENSP00000237596.2:n.595+213T>C
ENST00000237596.6:c.595+213T>C	ENSP00000237596.2:n.595+213T>C
ENST00000506727.1:n.97+213T>C
NM_000297.3:c.595+213T>C	NP_000288.1:n.595+213T>C
XM_011532028.1:c.595+213T>C	XP_011530330.1:n.595+213T>C
XR_244632.2:n.690+213T>C
NR_156488.1:n.682+213T>C
XM_011532028.2:c.595+213T>C	XP_011530330.1:n.595+213T>C
NM_000297.4:c.595+213T>C MANE Select	NP_000288.1:n.595+213T>C
NR_156488.2:n.694+213T>C