Canonical Allele Identifier: CA679974507
Gene: FOLR1 HGNC NCBI

Linked Data

dbSNP Id: rs1189343808
MyVariant Identifiers: chr11:g.71900779G>C (hg19) chr11:g.72189735G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72189735G>C , CM000673.2:g.72189735G>C GRCh38
NC_000011.9:g.71900779G>C , CM000673.1:g.71900779G>C GRCh37
NC_000011.8:g.71578427G>C NCBI36
NG_015863.1:g.5178G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000312293.9:c.-33G>C ENSP00000308137.4:n.-33G>C
ENST00000312293.8:c.-33G>C ENSP00000308137.4:n.-33G>C
ENST00000393681.6:c.-99G>C ENSP00000377286.2:n.-99G>C
NM_016724.2:c.-99G>C NP_057936.1:n.-99G>C
NM_016725.2:c.-33G>C NP_057937.1:n.-33G>C
NM_016724.3:c.-99G>C NP_057936.1:n.-99G>C
NM_016725.3:c.-33G>C NP_057937.1:n.-33G>C
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