Canonical Allele Identifier: CA440296666

Gene: PKD2

Linked Data

• MyVariant Identifiers: chr4:g.88929098C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88007946C>G , CM000666.2:g.88007946C>G	GRCh38
NC_000004.11:g.88929098C>G , CM000666.1:g.88929098C>G	GRCh37
NC_000004.10:g.89148122C>G	NCBI36
NG_008604.1:g.5279C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.213C>G MANE Select	ENSP00000237596.2:p.Ala71=
ENST00000237596.6:c.213C>G	ENSP00000237596.2:p.Ala71=
NM_000297.3:c.213C>G	NP_000288.1:p.Ala71=
XM_011532028.1:c.213C>G	XP_011530330.1:p.Ala71=
XR_244632.2:n.308C>G
NR_156488.1:n.300C>G
XM_011532028.2:c.213C>G	XP_011530330.1:p.Ala71=
NM_000297.4:c.213C>G MANE Select	NP_000288.1:p.Ala71=
NR_156488.2:n.312C>G