Canonical Allele Identifier: CA2667924837

Gene: FOXL2

Linked Data

• gnomAD v4: 3-138945355-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.138945356dup , CM000665.2:g.138945356dup	GRCh38
NC_000003.11:g.138664198dup , CM000665.1:g.138664198dup	GRCh37
NC_000003.10:g.140146888dup	NCBI36
NG_012454.1:g.6785dup
NG_029796.1:g.3123dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648323.1:c.*236dup MANE Select	ENSP00000497217.1:n.*236dup
ENST00000330315.3:c.*236dup	ENSP00000333188.3:n.*236dup
NM_023067.3:c.*236dup	NP_075555.1:n.*236dup
NM_023067.4:c.*236dup MANE Select	NP_075555.1:n.*236dup