Canonical Allele Identifier: CA37515368
Gene: PROX1 HGNC NCBI
PROX1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs765346585
MyVariant Identifiers: chr1:g.214158942G>T (hg19) chr1:g.213985599G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213985599G>T , CM000663.2:g.213985599G>T GRCh38
NC_000001.10:g.214158942G>T , CM000663.1:g.214158942G>T GRCh37
NC_000001.9:g.212225565G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471129.1:c.-68+2276G>T (PROX1) ENSP00000419517.1:n.-68+2276G>T
NR_037850.2:n.85+470C>A (PROX1-AS1)
XM_011509773.1:c.-68+2276G>T (PROX1) XP_011508075.1:n.-68+2276G>T
XM_011509773.2:c.-68+2276G>T (PROX1) XP_011508075.1:n.-68+2276G>T
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