Canonical Allele Identifier: CA1405402622
Gene: FOXL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946658C= , CM000665.2:g.138946658C= GRCh38
NC_000003.11:g.138665500C= , CM000665.1:g.138665500C= GRCh37
NC_000003.10:g.140148190C= NCBI36
NG_012454.1:g.5483G=
NG_029796.1:g.4425C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.65G= MANE Select ENSP00000497217.1:p.Arg22=
ENST00000330315.3:c.65G= ENSP00000333188.3:p.Arg22=
NM_023067.3:c.65G= NP_075555.1:p.Arg22=
NM_023067.4:c.65G= MANE Select NP_075555.1:p.Arg22=
Search 100 bp 5'
Search 100 bp 3'