Canonical Allele Identifier: CA381732977

Gene: FOLR1

Linked Data

• ClinVar Variation Id: 2111064
• ClinVar RCV Id: RCV003023861
• MyVariant Identifiers: chr11:g.71906664G>C (hg19) ; chr11:g.72195620G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72195620G>C , CM000673.2:g.72195620G>C	GRCh38
NC_000011.9:g.71906664G>C , CM000673.1:g.71906664G>C	GRCh37
NC_000011.8:g.71584312G>C	NCBI36
NG_015863.1:g.11063G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312293.9:c.366G>C	ENSP00000308137.4:p.Gln122His
ENST00000393676.5:c.366G>C MANE Select	ENSP00000377281.3:p.Gln122His
ENST00000675784.1:c.366G>C	ENSP00000502440.1:p.Gln122His
ENST00000312293.8:c.366G>C	ENSP00000308137.4:p.Gln122His
ENST00000393676.3:c.366G>C	ENSP00000377281.3:p.Gln122His
ENST00000393679.5:c.366G>C	ENSP00000377284.1:p.Gln122His
ENST00000393681.6:c.366G>C	ENSP00000377286.2:p.Gln122His
NM_000802.3:c.366G>C	NP_000793.1:p.Gln122His
NM_016724.2:c.366G>C	NP_057936.1:p.Gln122His
NM_016725.2:c.366G>C	NP_057937.1:p.Gln122His
NM_016729.2:c.366G>C	NP_057941.1:p.Gln122His
NM_016729.3:c.366G>C MANE Select	NP_057941.1:p.Gln122His
NM_016724.3:c.366G>C	NP_057936.1:p.Gln122His
NM_016725.3:c.366G>C	NP_057937.1:p.Gln122His