Canonical Allele Identifier: CA679924059

Gene: FOLR3

Linked Data

• dbSNP Id: rs1264481413
• gnomAD v3: 11-72134419-T-C
• gnomAD v4: 11-72134419-T-C
• MyVariant Identifiers: chr11:g.71845465T>C (hg19) ; chr11:g.72134419T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72134419T>C , CM000673.2:g.72134419T>C	GRCh38
NC_000011.9:g.71845465T>C , CM000673.1:g.71845465T>C	GRCh37
NC_000011.8:g.71523113T>C	NCBI36
NG_032935.1:g.3695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622388.4:c.-6-1528T>C	ENSP00000481833.1:n.-6-1528T>C