Canonical Allele Identifier: CA1405402564

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138946554A= , CM000665.2:g.138946554A=	GRCh38
NC_000003.11:g.138665396A= , CM000665.1:g.138665396A=	GRCh37
NC_000003.10:g.140148086A=	NCBI36
NG_012454.1:g.5587T=
NG_029796.1:g.4321A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000648323.1:c.169T= MANE Select	ENSP00000497217.1:p.Tyr57=
ENST00000330315.3:c.169T=	ENSP00000333188.3:p.Tyr57=
NM_023067.3:c.169T=	NP_075555.1:p.Tyr57=
NM_023067.4:c.169T= MANE Select	NP_075555.1:p.Tyr57=