Canonical Allele Identifier: CA224393638
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs997472640
gnomAD v3: 11-72134446-T-G
gnomAD v4: 11-72134446-T-G
MyVariant Identifiers: chr11:g.71845492T>G (hg19) chr11:g.72134446T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134446T>G , CM000673.2:g.72134446T>G GRCh38
NC_000011.9:g.71845492T>G , CM000673.1:g.71845492T>G GRCh37
NC_000011.8:g.71523140T>G NCBI36
NG_032935.1:g.3722T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1501T>G ENSP00000481833.1:n.-6-1501T>G
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