Canonical Allele Identifier: CA224393606
Gene: FOLR3 HGNC NCBI

Linked Data

dbSNP Id: rs1027748630
MyVariant Identifiers: chr11:g.72134402A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72134402A>G , CM000673.2:g.72134402A>G GRCh38
NC_000011.9:g.71845448A>G , CM000673.1:g.71845448A>G GRCh37
NC_000011.8:g.71523096A>G NCBI36
NG_032935.1:g.3678A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622388.4:c.-6-1545A>G ENSP00000481833.1:n.-6-1545A>G