Canonical Allele Identifier: CA475606013

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929751A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218707A>G , CM000673.2:g.72218707A>G	GRCh38
NC_000011.9:g.71929751A>G , CM000673.1:g.71929751A>G	GRCh37
NC_000011.8:g.71607399A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298223.11:c.123A>G MANE Select	ENSP00000298223.6:p.Pro41=
ENST00000298223.10:c.123A>G	ENSP00000298223.6:p.Pro41=
ENST00000321324.11:c.162A>G	ENSP00000321957.7:p.Pro54=
ENST00000449475.6:c.174A>G	ENSP00000405638.2:p.Pro58=
ENST00000454954.6:c.27+1782A>G	ENSP00000414094.2:n.27+1782A>G
ENST00000535625.5:c.123A>G	ENSP00000444794.1:p.Pro41=
ENST00000536778.5:c.168A>G	ENSP00000438568.1:p.Pro56=
ENST00000538353.1:c.123A>G	ENSP00000440337.1:p.Pro41=
ENST00000539412.5:c.156A>G	ENSP00000441547.1:p.Pro52=
ENST00000541003.5:c.261A>G	ENSP00000443307.1:p.Pro87=
ENST00000619261.4:c.174A>G	ENSP00000480592.1:p.Pro58=
NM_000803.4:c.123A>G	NP_000794.3:p.Pro41=
NM_001113534.1:c.123A>G	NP_001107006.1:p.Pro41=
NM_001113535.1:c.123A>G	NP_001107007.1:p.Pro41=
NM_001113536.1:c.123A>G	NP_001107008.1:p.Pro41=
XM_005273856.2:c.150A>G	XP_005273913.1:p.Pro50=
XM_011544869.1:c.174A>G	XP_011543171.1:p.Pro58=
XM_011544870.1:c.168A>G	XP_011543172.1:p.Pro56=
XM_011544871.1:c.162A>G	XP_011543173.1:p.Pro54=
XM_011544872.1:c.156A>G	XP_011543174.1:p.Pro52=
XM_005273856.4:c.150A>G	XP_005273913.1:p.Pro50=
XM_024448412.1:c.174A>G	XP_024304180.1:p.Pro58=
NM_000803.5:c.123A>G MANE Select	NP_000794.3:p.Pro41=
NM_001113534.2:c.123A>G	NP_001107006.1:p.Pro41=
NM_001113535.2:c.123A>G	NP_001107007.1:p.Pro41=
NM_001113536.2:c.123A>G	NP_001107008.1:p.Pro41=