Canonical Allele Identifier: CA381743642

Gene: FOLR2

Linked Data

• dbSNP Id: rs1948432519
• gnomAD v3: 11-72218631-C-A
• gnomAD v4: 11-72218631-C-A
• MyVariant Identifiers: chr11:g.71929675C>A (hg19) ; chr11:g.72218631C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218631C>A , CM000673.2:g.72218631C>A	GRCh38
NC_000011.9:g.71929675C>A , CM000673.1:g.71929675C>A	GRCh37
NC_000011.8:g.71607323C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.47C>A MANE Select	ENSP00000298223.6:p.Ala16Asp
ENST00000298223.10:c.47C>A	ENSP00000298223.6:p.Ala16Asp
ENST00000321324.11:c.86C>A	ENSP00000321957.7:p.Ala29Asp
ENST00000449475.6:c.98C>A	ENSP00000405638.2:p.Ala33Asp
ENST00000454954.6:c.27+1706C>A	ENSP00000414094.2:n.27+1706C>A
ENST00000535625.5:c.47C>A	ENSP00000444794.1:p.Ala16Asp
ENST00000536778.5:c.92C>A	ENSP00000438568.1:p.Ala31Asp
ENST00000538353.1:c.47C>A	ENSP00000440337.1:p.Ala16Asp
ENST00000539412.5:c.80C>A	ENSP00000441547.1:p.Ala27Asp
ENST00000541003.5:c.185C>A	ENSP00000443307.1:p.Ala62Asp
ENST00000619261.4:c.98C>A	ENSP00000480592.1:p.Ala33Asp
NM_000803.4:c.47C>A	NP_000794.3:p.Ala16Asp
NM_001113534.1:c.47C>A	NP_001107006.1:p.Ala16Asp
NM_001113535.1:c.47C>A	NP_001107007.1:p.Ala16Asp
NM_001113536.1:c.47C>A	NP_001107008.1:p.Ala16Asp
XM_005273856.2:c.74C>A	XP_005273913.1:p.Ala25Asp
XM_011544869.1:c.98C>A	XP_011543171.1:p.Ala33Asp
XM_011544870.1:c.92C>A	XP_011543172.1:p.Ala31Asp
XM_011544871.1:c.86C>A	XP_011543173.1:p.Ala29Asp
XM_011544872.1:c.80C>A	XP_011543174.1:p.Ala27Asp
XM_005273856.4:c.74C>A	XP_005273913.1:p.Ala25Asp
XM_024448412.1:c.98C>A	XP_024304180.1:p.Ala33Asp
NM_000803.5:c.47C>A MANE Select	NP_000794.3:p.Ala16Asp
NM_001113534.2:c.47C>A	NP_001107006.1:p.Ala16Asp
NM_001113535.2:c.47C>A	NP_001107007.1:p.Ala16Asp
NM_001113536.2:c.47C>A	NP_001107008.1:p.Ala16Asp