Canonical Allele Identifier: CA1405402201
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945857T= , CM000665.2:g.138945857T= GRCh38
NC_000003.11:g.138664699T= , CM000665.1:g.138664699T= GRCh37
NC_000003.10:g.140147389T= NCBI36
NG_012454.1:g.6284A=
NG_029796.1:g.3624T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.866A= MANE Select ENSP00000497217.1:p.His289=
ENST00000330315.3:c.866A= ENSP00000333188.3:p.His289=
NM_023067.3:c.866A= NP_075555.1:p.His289=
NM_023067.4:c.866A= MANE Select NP_075555.1:p.His289=