Canonical Allele Identifier: CA381744230

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929734C>T (hg19) ; chr11:g.72218690C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218690C>T , CM000673.2:g.72218690C>T	GRCh38
NC_000011.9:g.71929734C>T , CM000673.1:g.71929734C>T	GRCh37
NC_000011.8:g.71607382C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298223.11:c.106C>T MANE Select	ENSP00000298223.6:p.His36Tyr
ENST00000298223.10:c.106C>T	ENSP00000298223.6:p.His36Tyr
ENST00000321324.11:c.145C>T	ENSP00000321957.7:p.His49Tyr
ENST00000449475.6:c.157C>T	ENSP00000405638.2:p.His53Tyr
ENST00000454954.6:c.27+1765C>T	ENSP00000414094.2:n.27+1765C>T
ENST00000535625.5:c.106C>T	ENSP00000444794.1:p.His36Tyr
ENST00000536778.5:c.151C>T	ENSP00000438568.1:p.His51Tyr
ENST00000538353.1:c.106C>T	ENSP00000440337.1:p.His36Tyr
ENST00000539412.5:c.139C>T	ENSP00000441547.1:p.His47Tyr
ENST00000541003.5:c.244C>T	ENSP00000443307.1:p.His82Tyr
ENST00000619261.4:c.157C>T	ENSP00000480592.1:p.His53Tyr
NM_000803.4:c.106C>T	NP_000794.3:p.His36Tyr
NM_001113534.1:c.106C>T	NP_001107006.1:p.His36Tyr
NM_001113535.1:c.106C>T	NP_001107007.1:p.His36Tyr
NM_001113536.1:c.106C>T	NP_001107008.1:p.His36Tyr
XM_005273856.2:c.133C>T	XP_005273913.1:p.His45Tyr
XM_011544869.1:c.157C>T	XP_011543171.1:p.His53Tyr
XM_011544870.1:c.151C>T	XP_011543172.1:p.His51Tyr
XM_011544871.1:c.145C>T	XP_011543173.1:p.His49Tyr
XM_011544872.1:c.139C>T	XP_011543174.1:p.His47Tyr
XM_005273856.4:c.133C>T	XP_005273913.1:p.His45Tyr
XM_024448412.1:c.157C>T	XP_024304180.1:p.His53Tyr
NM_000803.5:c.106C>T MANE Select	NP_000794.3:p.His36Tyr
NM_001113534.2:c.106C>T	NP_001107006.1:p.His36Tyr
NM_001113535.2:c.106C>T	NP_001107007.1:p.His36Tyr
NM_001113536.2:c.106C>T	NP_001107008.1:p.His36Tyr