Canonical Allele Identifier: CA16042767
Gene: FOLR1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372855
ClinVar RCV Id: RCV000414186
dbSNP Id: rs1057518027

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195460G>A , CM000673.2:g.72195460G>A GRCh38
NC_000011.9:g.71906504G>A , CM000673.1:g.71906504G>A GRCh37
NC_000011.8:g.71584152G>A NCBI36
NG_015863.1:g.10903G>A

Transcript Alleles

HGVS Amino-acid change
NM_000802.3:c.357+1G>A VV NP_000793.1:p.=
NM_016724.2:c.357+1G>A VV NP_057936.1:p.=
NM_016725.2:c.357+1G>A VV NP_057937.1:p.=
NM_016729.2:c.357+1G>A VV NP_057941.1:p.=
NM_016729.3:c.357+1G>A VV MANE Preferred
ENST00000312293.8:c.357+1G>A ENSP00000308137.4:p.=
ENST00000393676.3:c.357+1G>A ENSP00000377281.3:p.=
ENST00000393679.5:c.357+1G>A ENSP00000377284.1:p.=
ENST00000393681.6:c.357+1G>A ENSP00000377286.2:p.=