Canonical Allele Identifier: CA354703368
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2255427
ClinVar RCV Id: RCV002772315

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945915C>A , CM000665.2:g.138945915C>A GRCh38
NC_000003.11:g.138664757C>A , CM000665.1:g.138664757C>A GRCh37
NC_000003.10:g.140147447C>A NCBI36
NG_012454.1:g.6226G>T
NG_029796.1:g.3682C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.808G>T MANE Select ENSP00000497217.1:p.Val270Leu
ENST00000330315.3:c.808G>T ENSP00000333188.3:p.Val270Leu
NM_023067.3:c.808G>T NP_075555.1:p.Val270Leu
NM_023067.4:c.808G>T MANE Select NP_075555.1:p.Val270Leu