Canonical Allele Identifier: CA224393725

Gene: FOLR3

Linked Data

• dbSNP Id: rs200566509
• gnomAD v3: 11-72134696-CTG-C
• gnomAD v4: 11-72134696-CTG-C
• MyVariant Identifiers: chr11:g.71845743_71845744del (hg19) ; chr11:g.72134697_72134698del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72134698_72134699del , CM000673.2:g.72134698_72134699del	GRCh38
NC_000011.9:g.71845744_71845745del , CM000673.1:g.71845744_71845745del	GRCh37
NC_000011.8:g.71523392_71523393del	NCBI36
NG_032935.1:g.3974_3975del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622388.4:c.-6-1249_-6-1248del	ENSP00000481833.1:n.-6-1249_-6-1248del