Canonical Allele Identifier: CA224393602
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs973867884
gnomAD v3: 11-72134397-T-C
gnomAD v4: 11-72134397-T-C
MyVariant Identifiers: chr11:g.71845443T>C (hg19) chr11:g.72134397T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134397T>C , CM000673.2:g.72134397T>C GRCh38
NC_000011.9:g.71845443T>C , CM000673.1:g.71845443T>C GRCh37
NC_000011.8:g.71523091T>C NCBI36
NG_032935.1:g.3673T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1550T>C ENSP00000481833.1:n.-6-1550T>C
Search 100 bp 5'
Search 100 bp 3'