Canonical Allele Identifier: CA1405402222

Gene: FOXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945901G= , CM000665.2:g.138945901G=	GRCh38
NC_000003.11:g.138664743G= , CM000665.1:g.138664743G=	GRCh37
NC_000003.10:g.140147433G=	NCBI36
NG_012454.1:g.6240C=
NG_029796.1:g.3668G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.822C= MANE Select	ENSP00000497217.1:p.Tyr274=
ENST00000330315.3:c.822C=	ENSP00000333188.3:p.Tyr274=
NM_023067.3:c.822C=	NP_075555.1:p.Tyr274=
NM_023067.4:c.822C= MANE Select	NP_075555.1:p.Tyr274=