Canonical Allele Identifier: CA16042767
Gene: FOLR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372855
ClinVar RCV Id: RCV000414186
dbSNP Id: rs1057518027
MyVariant Identifiers: chr11:g.71906504G>A (hg19) chr11:g.72195460G>A (hg38)
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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
ENST00000312293.9:c.357+1G>A ENSP00000308137.4:n.357+1G>A
ENST00000393676.5:c.357+1G>A MANE Select ENSP00000377281.3:n.357+1G>A
ENST00000675784.1:c.357+1G>A ENSP00000502440.1:n.357+1G>A
ENST00000312293.8:c.357+1G>A ENSP00000308137.4:n.357+1G>A
ENST00000393676.3:c.357+1G>A ENSP00000377281.3:n.357+1G>A
ENST00000393679.5:c.357+1G>A ENSP00000377284.1:n.357+1G>A
ENST00000393681.6:c.357+1G>A ENSP00000377286.2:n.357+1G>A
NM_000802.3:c.357+1G>A NP_000793.1:n.357+1G>A
NM_016724.2:c.357+1G>A NP_057936.1:n.357+1G>A
NM_016725.2:c.357+1G>A NP_057937.1:n.357+1G>A
NM_016729.2:c.357+1G>A NP_057941.1:n.357+1G>A
NM_016729.3:c.357+1G>A MANE Select NP_057941.1:n.357+1G>A
NM_016724.3:c.357+1G>A NP_057936.1:n.357+1G>A
NM_016725.3:c.357+1G>A NP_057937.1:n.357+1G>A
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