Canonical Allele Identifier: CA37515363
Gene: PROX1 HGNC NCBI
PROX1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs887946407
gnomAD v3: 1-213985593-T-G
gnomAD v4: 1-213985593-T-G
MyVariant Identifiers: chr1:g.214158936T>G (hg19) chr1:g.213985593T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213985593T>G , CM000663.2:g.213985593T>G GRCh38
NC_000001.10:g.214158936T>G , CM000663.1:g.214158936T>G GRCh37
NC_000001.9:g.212225559T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471129.1:c.-68+2270T>G (PROX1) ENSP00000419517.1:n.-68+2270T>G
NR_037850.2:n.85+476A>C (PROX1-AS1)
XM_011509773.1:c.-68+2270T>G (PROX1) XP_011508075.1:n.-68+2270T>G
XM_011509773.2:c.-68+2270T>G (PROX1) XP_011508075.1:n.-68+2270T>G
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