Canonical Allele Identifier: CA440296772
Gene: PKD2 HGNC NCBI

Linked Data

dbSNP Id: rs1472502781
gnomAD v2: 4-88929194-G-T
gnomAD v4: 4-88008042-G-T
MyVariant Identifiers: chr4:g.88929194G>T (hg19) chr4:g.88008042G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008042G>T , CM000666.2:g.88008042G>T GRCh38
NC_000004.11:g.88929194G>T , CM000666.1:g.88929194G>T GRCh37
NC_000004.10:g.89148218G>T NCBI36
NG_008604.1:g.5375G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.309G>T MANE Select ENSP00000237596.2:p.Val103=
ENST00000237596.6:c.309G>T ENSP00000237596.2:p.Val103=
NM_000297.3:c.309G>T NP_000288.1:p.Val103=
XM_011532028.1:c.309G>T XP_011530330.1:p.Val103=
XR_244632.2:n.404G>T
NR_156488.1:n.396G>T
XM_011532028.2:c.309G>T XP_011530330.1:p.Val103=
NM_000297.4:c.309G>T MANE Select NP_000288.1:p.Val103=
NR_156488.2:n.408G>T
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