Canonical Allele Identifier: CA224393683
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs115630330
gnomAD v2: 11-71845671-G-A
gnomAD v3: 11-72134625-G-A
gnomAD v4: 11-72134625-G-A
MyVariant Identifiers: chr11:g.71845671G>A (hg19) chr11:g.72134625G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134625G>A , CM000673.2:g.72134625G>A GRCh38
NC_000011.9:g.71845671G>A , CM000673.1:g.71845671G>A GRCh37
NC_000011.8:g.71523319G>A NCBI36
NG_032935.1:g.3901G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1322G>A ENSP00000481833.1:n.-6-1322G>A
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