Canonical Allele Identifier: CA799592468

Gene: PKD2

Linked Data

• dbSNP Id: rs1335599851
• gnomAD v4: 4-88007701-C-T
• MyVariant Identifiers: chr4:g.88928853C>T (hg19) ; chr4:g.88007701C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88007701C>T , CM000666.2:g.88007701C>T	GRCh38
NC_000004.11:g.88928853C>T , CM000666.1:g.88928853C>T	GRCh37
NC_000004.10:g.89147877C>T	NCBI36
NG_008604.1:g.5034C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.-33C>T MANE Select	ENSP00000237596.2:n.-33C>T
ENST00000237596.6:c.-33C>T	ENSP00000237596.2:n.-33C>T
NM_000297.3:c.-33C>T	NP_000288.1:n.-33C>T
XM_011532028.1:c.-33C>T	XP_011530330.1:n.-33C>T
XR_244632.2:n.63C>T
NR_156488.1:n.55C>T
XM_011532028.2:c.-33C>T	XP_011530330.1:n.-33C>T
NM_000297.4:c.-33C>T MANE Select	NP_000288.1:n.-33C>T
NR_156488.2:n.67C>T