Canonical Allele Identifier: CA440297153

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88929431G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88008279G>C , CM000666.2:g.88008279G>C	GRCh38
NC_000004.11:g.88929431G>C , CM000666.1:g.88929431G>C	GRCh37
NC_000004.10:g.89148455G>C	NCBI36
NG_008604.1:g.5612G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.546G>C MANE Select	ENSP00000237596.2:p.Gly182=
ENST00000237596.6:c.546G>C	ENSP00000237596.2:p.Gly182=
ENST00000506727.1:n.48G>C
NM_000297.3:c.546G>C	NP_000288.1:p.Gly182=
XM_011532028.1:c.546G>C	XP_011530330.1:p.Gly182=
XR_244632.2:n.641G>C
NR_156488.1:n.633G>C
XM_011532028.2:c.546G>C	XP_011530330.1:p.Gly182=
NM_000297.4:c.546G>C MANE Select	NP_000288.1:p.Gly182=
NR_156488.2:n.645G>C