Canonical Allele Identifier: CA440268295
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1242420595
gnomAD v2: 4-88928906-G-C
gnomAD v3: 4-88007754-G-C
gnomAD v4: 4-88007754-G-C
MyVariant Identifiers: chr4:g.88928906G>C (hg19) chr4:g.88007754G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88007754G>C , CM000666.2:g.88007754G>C GRCh38
NC_000004.11:g.88928906G>C , CM000666.1:g.88928906G>C GRCh37
NC_000004.10:g.89147930G>C NCBI36
NG_008604.1:g.5087G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.21G>C MANE Select ENSP00000237596.2:p.Val7=
ENST00000237596.6:c.21G>C ENSP00000237596.2:p.Val7=
NM_000297.3:c.21G>C NP_000288.1:p.Val7=
XM_011532028.1:c.21G>C XP_011530330.1:p.Val7=
XR_244632.2:n.116G>C
NR_156488.1:n.108G>C
XM_011532028.2:c.21G>C XP_011530330.1:p.Val7=
NM_000297.4:c.21G>C MANE Select NP_000288.1:p.Val7=
NR_156488.2:n.120G>C
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