Canonical Allele Identifier: CA11639143
Gene: PROM1 HGNC NCBI
FGFBP2 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.15963240G>T
GRCh37 chr4:g.15964863G>T
gnomAD v2:
4:15964863 G / T
gnomAD v3:
4:15963240 G / T
gnomAD v4:
chr4-15963240-G-T
Joint Max Group AF 0.5266461 (SAS)
Genomes Max Group AF 0.52621887 (SAS)
Exomes Max Group AF 0.54171156 (AMR)
dbSNP:
4698433
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.15963240G>T , CM000666.2:g.15963240G>T GRCh38
NC_000004.11:g.15964863G>T , CM000666.1:g.15964863G>T GRCh37
NC_000004.10:g.15573961G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000503884.5:c.539-81C>A (PROM1)
ENST00000509331.1:n.83-2629C>A (FGFBP2)
Search 100 bp 5'
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