Canonical Allele Identifier: CA679924046
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1202449149
MyVariant Identifiers: chr11:g.71845450G>A (hg19) chr11:g.72134404G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134404G>A , CM000673.2:g.72134404G>A GRCh38
NC_000011.9:g.71845450G>A , CM000673.1:g.71845450G>A GRCh37
NC_000011.8:g.71523098G>A NCBI36
NG_032935.1:g.3680G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1543G>A ENSP00000481833.1:n.-6-1543G>A
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