Canonical Allele Identifier: CA799607527

Gene: PKD2

Linked Data

• dbSNP Id: rs2725221
• MyVariant Identifiers: chr4:g.88959381G>C (hg19) ; chr4:g.88038229G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038229G>C , CM000666.2:g.88038229G>C	GRCh38
NC_000004.11:g.88959381G>C , CM000666.1:g.88959381G>C	GRCh37
NC_000004.10:g.89178405G>C	NCBI36
NG_008604.1:g.35562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.844-22G>C MANE Select	ENSP00000237596.2:n.844-22G>C
ENST00000237596.6:c.844-22G>C	ENSP00000237596.2:n.844-22G>C
ENST00000506367.1:n.291-22G>C
ENST00000506727.1:n.430-22G>C
NM_000297.3:c.844-22G>C	NP_000288.1:n.844-22G>C
XM_011532028.1:c.844-22G>C	XP_011530330.1:n.844-22G>C
XM_011532029.1:c.124-22G>C	XP_011530331.1:n.124-22G>C
XM_011532030.1:c.4-22G>C	XP_011530332.1:n.4-22G>C
XR_244632.2:n.939-22G>C
NR_156488.1:n.931-22G>C
XM_011532028.2:c.844-22G>C	XP_011530330.1:n.844-22G>C
XM_011532030.2:c.4-22G>C	XP_011530332.1:n.4-22G>C
NM_000297.4:c.844-22G>C MANE Select	NP_000288.1:n.844-22G>C
NR_156488.2:n.943-22G>C