Canonical Allele Identifier: CA528921813
Gene: PROX1 HGNC NCBI
PROX1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1249628630
gnomAD v2: 1-214158980-G-C
gnomAD v3: 1-213985637-G-C
gnomAD v4: 1-213985637-G-C
MyVariant Identifiers: chr1:g.214158980G>C (hg19) chr1:g.213985637G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213985637G>C , CM000663.2:g.213985637G>C GRCh38
NC_000001.10:g.214158980G>C , CM000663.1:g.214158980G>C GRCh37
NC_000001.9:g.212225603G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000471129.1:c.-68+2314G>C (PROX1) ENSP00000419517.1:n.-68+2314G>C
NR_037850.2:n.85+432C>G (PROX1-AS1)
XM_011509773.1:c.-68+2314G>C (PROX1) XP_011508075.1:n.-68+2314G>C
XM_011509773.2:c.-68+2314G>C (PROX1) XP_011508075.1:n.-68+2314G>C
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