Canonical Allele Identifier: CA475606001

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929739C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218695C>T , CM000673.2:g.72218695C>T	GRCh38
NC_000011.9:g.71929739C>T , CM000673.1:g.71929739C>T	GRCh37
NC_000011.8:g.71607387C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298223.11:c.111C>T MANE Select	ENSP00000298223.6:p.His37=
ENST00000298223.10:c.111C>T	ENSP00000298223.6:p.His37=
ENST00000321324.11:c.150C>T	ENSP00000321957.7:p.His50=
ENST00000449475.6:c.162C>T	ENSP00000405638.2:p.His54=
ENST00000454954.6:c.27+1770C>T	ENSP00000414094.2:n.27+1770C>T
ENST00000535625.5:c.111C>T	ENSP00000444794.1:p.His37=
ENST00000536778.5:c.156C>T	ENSP00000438568.1:p.His52=
ENST00000538353.1:c.111C>T	ENSP00000440337.1:p.His37=
ENST00000539412.5:c.144C>T	ENSP00000441547.1:p.His48=
ENST00000541003.5:c.249C>T	ENSP00000443307.1:p.His83=
ENST00000619261.4:c.162C>T	ENSP00000480592.1:p.His54=
NM_000803.4:c.111C>T	NP_000794.3:p.His37=
NM_001113534.1:c.111C>T	NP_001107006.1:p.His37=
NM_001113535.1:c.111C>T	NP_001107007.1:p.His37=
NM_001113536.1:c.111C>T	NP_001107008.1:p.His37=
XM_005273856.2:c.138C>T	XP_005273913.1:p.His46=
XM_011544869.1:c.162C>T	XP_011543171.1:p.His54=
XM_011544870.1:c.156C>T	XP_011543172.1:p.His52=
XM_011544871.1:c.150C>T	XP_011543173.1:p.His50=
XM_011544872.1:c.144C>T	XP_011543174.1:p.His48=
XM_005273856.4:c.138C>T	XP_005273913.1:p.His46=
XM_024448412.1:c.162C>T	XP_024304180.1:p.His54=
NM_000803.5:c.111C>T MANE Select	NP_000794.3:p.His37=
NM_001113534.2:c.111C>T	NP_001107006.1:p.His37=
NM_001113535.2:c.111C>T	NP_001107007.1:p.His37=
NM_001113536.2:c.111C>T	NP_001107008.1:p.His37=