Canonical Allele Identifier: CA224393621
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs911928731
gnomAD v3: 11-72134425-T-C
gnomAD v4: 11-72134425-T-C
MyVariant Identifiers: chr11:g.71845471T>C (hg19) chr11:g.72134425T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134425T>C , CM000673.2:g.72134425T>C GRCh38
NC_000011.9:g.71845471T>C , CM000673.1:g.71845471T>C GRCh37
NC_000011.8:g.71523119T>C NCBI36
NG_032935.1:g.3701T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1522T>C ENSP00000481833.1:n.-6-1522T>C
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