Canonical Allele Identifier: CA381743367

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929633T>G (hg19) ; chr11:g.72218589T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218589T>G , CM000673.2:g.72218589T>G	GRCh38
NC_000011.9:g.71929633T>G , CM000673.1:g.71929633T>G	GRCh37
NC_000011.8:g.71607281T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298223.11:c.5T>G MANE Select	ENSP00000298223.6:p.Val2Gly
ENST00000298223.10:c.5T>G	ENSP00000298223.6:p.Val2Gly
ENST00000321324.11:c.44T>G	ENSP00000321957.7:p.Val15Gly
ENST00000449475.6:c.56T>G	ENSP00000405638.2:p.Val19Gly
ENST00000454954.6:c.27+1664T>G	ENSP00000414094.2:n.27+1664T>G
ENST00000535625.5:c.5T>G	ENSP00000444794.1:p.Val2Gly
ENST00000536778.5:c.50T>G	ENSP00000438568.1:p.Val17Gly
ENST00000538353.1:c.5T>G	ENSP00000440337.1:p.Val2Gly
ENST00000539412.5:c.38T>G	ENSP00000441547.1:p.Val13Gly
ENST00000541003.5:c.143T>G	ENSP00000443307.1:p.Val48Gly
ENST00000619261.4:c.56T>G	ENSP00000480592.1:p.Val19Gly
NM_000803.4:c.5T>G	NP_000794.3:p.Val2Gly
NM_001113534.1:c.5T>G	NP_001107006.1:p.Val2Gly
NM_001113535.1:c.5T>G	NP_001107007.1:p.Val2Gly
NM_001113536.1:c.5T>G	NP_001107008.1:p.Val2Gly
XM_005273856.2:c.32T>G	XP_005273913.1:p.Val11Gly
XM_011544869.1:c.56T>G	XP_011543171.1:p.Val19Gly
XM_011544870.1:c.50T>G	XP_011543172.1:p.Val17Gly
XM_011544871.1:c.44T>G	XP_011543173.1:p.Val15Gly
XM_011544872.1:c.38T>G	XP_011543174.1:p.Val13Gly
XM_005273856.4:c.32T>G	XP_005273913.1:p.Val11Gly
XM_024448412.1:c.56T>G	XP_024304180.1:p.Val19Gly
NM_000803.5:c.5T>G MANE Select	NP_000794.3:p.Val2Gly
NM_001113534.2:c.5T>G	NP_001107006.1:p.Val2Gly
NM_001113535.2:c.5T>G	NP_001107007.1:p.Val2Gly
NM_001113536.2:c.5T>G	NP_001107008.1:p.Val2Gly