Canonical Allele Identifier: CA285750
Gene: FOLR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 95750
dbSNP Id: rs144637717

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195749T>C , CM000673.2:g.72195749T>C GRCh38
NC_000011.9:g.71906793T>C , CM000673.1:g.71906793T>C GRCh37
NC_000011.8:g.71584441T>C NCBI36
NG_015863.1:g.11192T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.493+2T>C ENSP00000308137.4:n.493+2T>C
ENST00000393676.5:c.493+2T>C MANE Select ENSP00000377281.3:n.493+2T>C
ENST00000675784.1:c.493+2T>C ENSP00000502440.1:n.493+2T>C
ENST00000312293.8:c.493+2T>C ENSP00000308137.4:n.493+2T>C
ENST00000393676.3:c.493+2T>C ENSP00000377281.3:n.493+2T>C
ENST00000393679.5:c.493+2T>C ENSP00000377284.1:n.493+2T>C
ENST00000393681.6:c.493+2T>C ENSP00000377286.2:n.493+2T>C
NM_000802.3:c.493+2T>C NP_000793.1:n.493+2T>C
NM_016724.2:c.493+2T>C NP_057936.1:n.493+2T>C
NM_016725.2:c.493+2T>C NP_057937.1:n.493+2T>C
NM_016729.2:c.493+2T>C NP_057941.1:n.493+2T>C
NM_016729.3:c.493+2T>C MANE Select NP_057941.1:n.493+2T>C
NM_016724.3:c.493+2T>C NP_057936.1:n.493+2T>C
NM_016725.3:c.493+2T>C NP_057937.1:n.493+2T>C