Canonical Allele Identifier: CA440296773
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88008045-A-G
MyVariant Identifiers: chr4:g.88929197A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008045A>G , CM000666.2:g.88008045A>G GRCh38
NC_000004.11:g.88929197A>G , CM000666.1:g.88929197A>G GRCh37
NC_000004.10:g.89148221A>G NCBI36
NG_008604.1:g.5378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.312A>G MANE Select ENSP00000237596.2:p.Glu104=
ENST00000237596.6:c.312A>G ENSP00000237596.2:p.Glu104=
NM_000297.3:c.312A>G NP_000288.1:p.Glu104=
XM_011532028.1:c.312A>G XP_011530330.1:p.Glu104=
XR_244632.2:n.407A>G
NR_156488.1:n.399A>G
XM_011532028.2:c.312A>G XP_011530330.1:p.Glu104=
NM_000297.4:c.312A>G MANE Select NP_000288.1:p.Glu104=
NR_156488.2:n.411A>G