Canonical Allele Identifier: CA679924143

Gene: FOLR3

Linked Data

• dbSNP Id: rs1441646241
• gnomAD v3: 11-72134619-C-T
• gnomAD v4: 11-72134619-C-T
• MyVariant Identifiers: chr11:g.71845665C>T (hg19) ; chr11:g.72134619C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72134619C>T , CM000673.2:g.72134619C>T	GRCh38
NC_000011.9:g.71845665C>T , CM000673.1:g.71845665C>T	GRCh37
NC_000011.8:g.71523313C>T	NCBI36
NG_032935.1:g.3895C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622388.4:c.-6-1328C>T	ENSP00000481833.1:n.-6-1328C>T