Canonical Allele Identifier: CA440296449
Gene: PKD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.88928972G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007820G>C , CM000666.2:g.88007820G>C GRCh38
NC_000004.11:g.88928972G>C , CM000666.1:g.88928972G>C GRCh37
NC_000004.10:g.89147996G>C NCBI36
NG_008604.1:g.5153G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.87G>C MANE Select ENSP00000237596.2:p.Leu29=
ENST00000237596.6:c.87G>C ENSP00000237596.2:p.Leu29=
NM_000297.3:c.87G>C NP_000288.1:p.Leu29=
XM_011532028.1:c.87G>C XP_011530330.1:p.Leu29=
XR_244632.2:n.182G>C
NR_156488.1:n.174G>C
XM_011532028.2:c.87G>C XP_011530330.1:p.Leu29=
NM_000297.4:c.87G>C MANE Select NP_000288.1:p.Leu29=
NR_156488.2:n.186G>C
Search 100 bp 5'
Search 100 bp 3'