Canonical Allele Identifier: CA731201624
Gene: PROX1 HGNC NCBI
PROX1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1283717277
gnomAD v3: 1-213985656-C-T
gnomAD v4: 1-213985656-C-T
MyVariant Identifiers: chr1:g.214158999C>T (hg19) chr1:g.213985656C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213985656C>T , CM000663.2:g.213985656C>T GRCh38
NC_000001.10:g.214158999C>T , CM000663.1:g.214158999C>T GRCh37
NC_000001.9:g.212225622C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471129.1:c.-68+2333C>T (PROX1) ENSP00000419517.1:n.-68+2333C>T
NR_037850.2:n.85+413G>A (PROX1-AS1)
XM_011509773.1:c.-68+2333C>T (PROX1) XP_011508075.1:n.-68+2333C>T
XM_011509773.2:c.-68+2333C>T (PROX1) XP_011508075.1:n.-68+2333C>T
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