Canonical Allele Identifier: CA6169317

Gene: FOLR2

Linked Data

• ClinVar Variation Id: 2599845
• ClinVar RCV Id: RCV004343328
• dbSNP Id: rs765590759
• ExAC: 11:71929710 C / T
• gnomAD v2: 11-71929710-C-T
• gnomAD v3: 11-72218666-C-T
• gnomAD v4: 11-72218666-C-T
• MyVariant Identifiers: chr11:g.71929710C>T (hg19) ; chr11:g.72218666C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218666C>T , CM000673.2:g.72218666C>T	GRCh38
NC_000011.9:g.71929710C>T , CM000673.1:g.71929710C>T	GRCh37
NC_000011.8:g.71607358C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.82C>T MANE Select	ENSP00000298223.6:p.Leu28Phe
ENST00000298223.10:c.82C>T	ENSP00000298223.6:p.Leu28Phe
ENST00000321324.11:c.121C>T	ENSP00000321957.7:p.Leu41Phe
ENST00000449475.6:c.133C>T	ENSP00000405638.2:p.Leu45Phe
ENST00000454954.6:c.27+1741C>T	ENSP00000414094.2:n.27+1741C>T
ENST00000535625.5:c.82C>T	ENSP00000444794.1:p.Leu28Phe
ENST00000536778.5:c.127C>T	ENSP00000438568.1:p.Leu43Phe
ENST00000538353.1:c.82C>T	ENSP00000440337.1:p.Leu28Phe
ENST00000539412.5:c.115C>T	ENSP00000441547.1:p.Leu39Phe
ENST00000541003.5:c.220C>T	ENSP00000443307.1:p.Leu74Phe
ENST00000619261.4:c.133C>T	ENSP00000480592.1:p.Leu45Phe
NM_000803.4:c.82C>T	NP_000794.3:p.Leu28Phe
NM_001113534.1:c.82C>T	NP_001107006.1:p.Leu28Phe
NM_001113535.1:c.82C>T	NP_001107007.1:p.Leu28Phe
NM_001113536.1:c.82C>T	NP_001107008.1:p.Leu28Phe
XM_005273856.2:c.109C>T	XP_005273913.1:p.Leu37Phe
XM_011544869.1:c.133C>T	XP_011543171.1:p.Leu45Phe
XM_011544870.1:c.127C>T	XP_011543172.1:p.Leu43Phe
XM_011544871.1:c.121C>T	XP_011543173.1:p.Leu41Phe
XM_011544872.1:c.115C>T	XP_011543174.1:p.Leu39Phe
XM_005273856.4:c.109C>T	XP_005273913.1:p.Leu37Phe
XM_024448412.1:c.133C>T	XP_024304180.1:p.Leu45Phe
NM_000803.5:c.82C>T MANE Select	NP_000794.3:p.Leu28Phe
NM_001113534.2:c.82C>T	NP_001107006.1:p.Leu28Phe
NM_001113535.2:c.82C>T	NP_001107007.1:p.Leu28Phe
NM_001113536.2:c.82C>T	NP_001107008.1:p.Leu28Phe