Canonical Allele Identifier: CA224398907
Gene: FOLR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 510642
ClinVar RCV Id: RCV000613231
dbSNP Id: rs919336828
gnomAD v2: 11-71900782-G-A
gnomAD v3: 11-72189738-G-A
gnomAD v4: 11-72189738-G-A
MyVariant Identifiers: chr11:g.71900782G>A (hg19) chr11:g.72189738G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72189738G>A , CM000673.2:g.72189738G>A GRCh38
NC_000011.9:g.71900782G>A , CM000673.1:g.71900782G>A GRCh37
NC_000011.8:g.71578430G>A NCBI36
NG_015863.1:g.5181G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312293.9:c.-30G>A ENSP00000308137.4:n.-30G>A
ENST00000312293.8:c.-30G>A ENSP00000308137.4:n.-30G>A
ENST00000393681.6:c.-96G>A ENSP00000377286.2:n.-96G>A
NM_016724.2:c.-96G>A NP_057936.1:n.-96G>A
NM_016725.2:c.-30G>A NP_057937.1:n.-30G>A
NM_016724.3:c.-96G>A NP_057936.1:n.-96G>A
NM_016725.3:c.-30G>A NP_057937.1:n.-30G>A
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