Canonical Allele Identifier: CA381744266

Gene: FOLR2

Linked Data

• MyVariant Identifiers: chr11:g.71929738A>C (hg19) ; chr11:g.72218694A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72218694A>C , CM000673.2:g.72218694A>C	GRCh38
NC_000011.9:g.71929738A>C , CM000673.1:g.71929738A>C	GRCh37
NC_000011.8:g.71607386A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000298223.11:c.110A>C MANE Select	ENSP00000298223.6:p.His37Pro
ENST00000298223.10:c.110A>C	ENSP00000298223.6:p.His37Pro
ENST00000321324.11:c.149A>C	ENSP00000321957.7:p.His50Pro
ENST00000449475.6:c.161A>C	ENSP00000405638.2:p.His54Pro
ENST00000454954.6:c.27+1769A>C	ENSP00000414094.2:n.27+1769A>C
ENST00000535625.5:c.110A>C	ENSP00000444794.1:p.His37Pro
ENST00000536778.5:c.155A>C	ENSP00000438568.1:p.His52Pro
ENST00000538353.1:c.110A>C	ENSP00000440337.1:p.His37Pro
ENST00000539412.5:c.143A>C	ENSP00000441547.1:p.His48Pro
ENST00000541003.5:c.248A>C	ENSP00000443307.1:p.His83Pro
ENST00000619261.4:c.161A>C	ENSP00000480592.1:p.His54Pro
NM_000803.4:c.110A>C	NP_000794.3:p.His37Pro
NM_001113534.1:c.110A>C	NP_001107006.1:p.His37Pro
NM_001113535.1:c.110A>C	NP_001107007.1:p.His37Pro
NM_001113536.1:c.110A>C	NP_001107008.1:p.His37Pro
XM_005273856.2:c.137A>C	XP_005273913.1:p.His46Pro
XM_011544869.1:c.161A>C	XP_011543171.1:p.His54Pro
XM_011544870.1:c.155A>C	XP_011543172.1:p.His52Pro
XM_011544871.1:c.149A>C	XP_011543173.1:p.His50Pro
XM_011544872.1:c.143A>C	XP_011543174.1:p.His48Pro
XM_005273856.4:c.137A>C	XP_005273913.1:p.His46Pro
XM_024448412.1:c.161A>C	XP_024304180.1:p.His54Pro
NM_000803.5:c.110A>C MANE Select	NP_000794.3:p.His37Pro
NM_001113534.2:c.110A>C	NP_001107006.1:p.His37Pro
NM_001113535.2:c.110A>C	NP_001107007.1:p.His37Pro
NM_001113536.2:c.110A>C	NP_001107008.1:p.His37Pro