Canonical Allele Identifier: CA475605728

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929634C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218590C>A , CM000673.2:g.72218590C>A	GRCh38
NC_000011.9:g.71929634C>A , CM000673.1:g.71929634C>A	GRCh37
NC_000011.8:g.71607282C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298223.11:c.6C>A MANE Select	ENSP00000298223.6:p.Val2=
ENST00000298223.10:c.6C>A	ENSP00000298223.6:p.Val2=
ENST00000321324.11:c.45C>A	ENSP00000321957.7:p.Val15=
ENST00000449475.6:c.57C>A	ENSP00000405638.2:p.Val19=
ENST00000454954.6:c.27+1665C>A	ENSP00000414094.2:n.27+1665C>A
ENST00000535625.5:c.6C>A	ENSP00000444794.1:p.Val2=
ENST00000536778.5:c.51C>A	ENSP00000438568.1:p.Val17=
ENST00000538353.1:c.6C>A	ENSP00000440337.1:p.Val2=
ENST00000539412.5:c.39C>A	ENSP00000441547.1:p.Val13=
ENST00000541003.5:c.144C>A	ENSP00000443307.1:p.Val48=
ENST00000619261.4:c.57C>A	ENSP00000480592.1:p.Val19=
NM_000803.4:c.6C>A	NP_000794.3:p.Val2=
NM_001113534.1:c.6C>A	NP_001107006.1:p.Val2=
NM_001113535.1:c.6C>A	NP_001107007.1:p.Val2=
NM_001113536.1:c.6C>A	NP_001107008.1:p.Val2=
XM_005273856.2:c.33C>A	XP_005273913.1:p.Val11=
XM_011544869.1:c.57C>A	XP_011543171.1:p.Val19=
XM_011544870.1:c.51C>A	XP_011543172.1:p.Val17=
XM_011544871.1:c.45C>A	XP_011543173.1:p.Val15=
XM_011544872.1:c.39C>A	XP_011543174.1:p.Val13=
XM_005273856.4:c.33C>A	XP_005273913.1:p.Val11=
XM_024448412.1:c.57C>A	XP_024304180.1:p.Val19=
NM_000803.5:c.6C>A MANE Select	NP_000794.3:p.Val2=
NM_001113534.2:c.6C>A	NP_001107006.1:p.Val2=
NM_001113535.2:c.6C>A	NP_001107007.1:p.Val2=
NM_001113536.2:c.6C>A	NP_001107008.1:p.Val2=