Canonical Allele Identifier: CA381731606
Gene: FOLR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1465705
ClinVar RCV Id: RCV001990345
dbSNP Id: rs1275551543

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72195278C>A , CM000673.2:g.72195278C>A GRCh38
NC_000011.9:g.71906322C>A , CM000673.1:g.71906322C>A GRCh37
NC_000011.8:g.71583970C>A NCBI36
NG_015863.1:g.10721C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312293.9:c.176C>A ENSP00000308137.4:p.Pro59His
ENST00000393676.5:c.176C>A MANE Select ENSP00000377281.3:p.Pro59His
ENST00000675784.1:c.176C>A ENSP00000502440.1:p.Pro59His
ENST00000312293.8:c.176C>A ENSP00000308137.4:p.Pro59His
ENST00000393676.3:c.176C>A ENSP00000377281.3:p.Pro59His
ENST00000393679.5:c.176C>A ENSP00000377284.1:p.Pro59His
ENST00000393681.6:c.176C>A ENSP00000377286.2:p.Pro59His
NM_000802.3:c.176C>A NP_000793.1:p.Pro59His
NM_016724.2:c.176C>A NP_057936.1:p.Pro59His
NM_016725.2:c.176C>A NP_057937.1:p.Pro59His
NM_016729.2:c.176C>A NP_057941.1:p.Pro59His
NM_016729.3:c.176C>A MANE Select NP_057941.1:p.Pro59His
NM_016724.3:c.176C>A NP_057936.1:p.Pro59His
NM_016725.3:c.176C>A NP_057937.1:p.Pro59His