Canonical Allele Identifier: CA737145188
Gene: PLPP3 HGNC NCBI

Linked Data

dbSNP Id: rs1354411487
gnomAD v3: 1-56500813-T-C
gnomAD v4: 1-56500813-T-C
MyVariant Identifiers: chr1:g.56966485T>C (hg19) chr1:g.56500813T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56500813T>C , CM000663.2:g.56500813T>C GRCh38
NC_000001.10:g.56966485T>C , CM000663.1:g.56966485T>C GRCh37
NC_000001.9:g.56739073T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371250.4:c.811-4137A>G MANE Select ENSP00000360296.3:n.811-4137A>G
ENST00000641109.1:c.220-4137A>G ENSP00000493138.1:n.220-4137A>G
ENST00000641494.1:c.65-4137A>G
ENST00000642129.1:c.455-4137A>G
ENST00000371250.3:c.811-4137A>G ENSP00000360296.3:n.811-4137A>G
ENST00000459962.1:n.1797-4137A>G
ENST00000472957.1:n.296-4137A>G
NM_003713.4:c.811-4137A>G NP_003704.3:n.811-4137A>G
NM_003713.5:c.811-4137A>G MANE Select NP_003704.3:n.811-4137A>G
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