Canonical Allele Identifier: CA100873621

Gene: PKD2

Linked Data

• dbSNP Id: rs1053400400
• MyVariant Identifiers: chr4:g.88929701C>T (hg19) ; chr4:g.88008549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88008549C>T , CM000666.2:g.88008549C>T	GRCh38
NC_000004.11:g.88929701C>T , CM000666.1:g.88929701C>T	GRCh37
NC_000004.10:g.89148725C>T	NCBI36
NG_008604.1:g.5882C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.595+221C>T MANE Select	ENSP00000237596.2:n.595+221C>T
ENST00000237596.6:c.595+221C>T	ENSP00000237596.2:n.595+221C>T
ENST00000506727.1:n.97+221C>T
NM_000297.3:c.595+221C>T	NP_000288.1:n.595+221C>T
XM_011532028.1:c.595+221C>T	XP_011530330.1:n.595+221C>T
XR_244632.2:n.690+221C>T
NR_156488.1:n.682+221C>T
XM_011532028.2:c.595+221C>T	XP_011530330.1:n.595+221C>T
NM_000297.4:c.595+221C>T MANE Select	NP_000288.1:n.595+221C>T
NR_156488.2:n.694+221C>T