Canonical Allele Identifier: CA600080189
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1365127369
gnomAD v2: 11-71845416-CTTAG-C
gnomAD v3: 11-72134370-CTTAG-C
gnomAD v4: 11-72134370-CTTAG-C
MyVariant Identifiers: chr11:g.71845417_71845420del (hg19) chr11:g.72134371_72134374del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134372_72134375del , CM000673.2:g.72134372_72134375del GRCh38
NC_000011.9:g.71845418_71845421del , CM000673.1:g.71845418_71845421del GRCh37
NC_000011.8:g.71523066_71523069del NCBI36
NG_032935.1:g.3648_3651del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1575_-6-1572del ENSP00000481833.1:n.-6-1575_-6-1572del
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