Canonical Allele Identifier: CA1405402465
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946330G= , CM000665.2:g.138946330G= GRCh38
NC_000003.11:g.138665172G= , CM000665.1:g.138665172G= GRCh37
NC_000003.10:g.140147862G= NCBI36
NG_012454.1:g.5811C=
NG_029796.1:g.4097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.393C= MANE Select ENSP00000497217.1:p.Asp131=
ENST00000330315.3:c.393C= ENSP00000333188.3:p.Asp131=
NM_023067.3:c.393C= NP_075555.1:p.Asp131=
NM_023067.4:c.393C= MANE Select NP_075555.1:p.Asp131=