Canonical Allele Identifier: CA2671365054
Gene: PKD2 HGNC NCBI

Linked Data

gnomAD v4: 4-88007671-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007671T>C , CM000666.2:g.88007671T>C GRCh38
NC_000004.11:g.88928823T>C , CM000666.1:g.88928823T>C GRCh37
NC_000004.10:g.89147847T>C NCBI36
NG_008604.1:g.5004T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.-63T>C MANE Select ENSP00000237596.2:n.-63T>C
ENST00000237596.6:c.-63T>C ENSP00000237596.2:n.-63T>C
NM_000297.3:c.-63T>C NP_000288.1:n.-63T>C
XM_011532028.1:c.-63T>C XP_011530330.1:n.-63T>C
XR_244632.2:n.33T>C
NR_156488.1:n.25T>C
XM_011532028.2:c.-63T>C XP_011530330.1:n.-63T>C
NM_000297.4:c.-63T>C MANE Select NP_000288.1:n.-63T>C
NR_156488.2:n.37T>C