Canonical Allele Identifier: CA679924024
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1478329756
gnomAD v3: 11-72134383-C-T
gnomAD v4: 11-72134383-C-T
MyVariant Identifiers: chr11:g.71845429C>T (hg19) chr11:g.72134383C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134383C>T , CM000673.2:g.72134383C>T GRCh38
NC_000011.9:g.71845429C>T , CM000673.1:g.71845429C>T GRCh37
NC_000011.8:g.71523077C>T NCBI36
NG_032935.1:g.3659C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1564C>T ENSP00000481833.1:n.-6-1564C>T
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