Canonical Allele Identifier: CA917019804

Gene: FOXL2

Linked Data

• dbSNP Id: rs1559921498

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945397_138945398del , CM000665.2:g.138945397_138945398del	GRCh38
NC_000003.11:g.138664239_138664240del , CM000665.1:g.138664239_138664240del	GRCh37
NC_000003.10:g.140146929_140146930del	NCBI36
NG_012454.1:g.6744_6745del
NG_029796.1:g.3164_3165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*195_*196del MANE Select	ENSP00000497217.1:n.*195_*196del
ENST00000330315.3:c.*195_*196del	ENSP00000333188.3:n.*195_*196del
NM_023067.3:c.*195_*196del	NP_075555.1:n.*195_*196del
NM_023067.4:c.*195_*196del MANE Select	NP_075555.1:n.*195_*196del