Canonical Allele Identifier: CA37515588
Gene: PROX1 HGNC NCBI
PROX1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1040721765
gnomAD v3: 1-213985808-T-A
gnomAD v4: 1-213985808-T-A
MyVariant Identifiers: chr1:g.214159151T>A (hg19) chr1:g.213985808T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213985808T>A , CM000663.2:g.213985808T>A GRCh38
NC_000001.10:g.214159151T>A , CM000663.1:g.214159151T>A GRCh37
NC_000001.9:g.212225774T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471129.1:c.-68+2485T>A (PROX1) ENSP00000419517.1:n.-68+2485T>A
NR_037850.2:n.85+261A>T (PROX1-AS1)
XM_011509773.1:c.-68+2485T>A (PROX1) XP_011508075.1:n.-68+2485T>A
XM_011509773.2:c.-68+2485T>A (PROX1) XP_011508075.1:n.-68+2485T>A
Search 100 bp 5'
Search 100 bp 3'