Canonical Allele Identifier: CA354699982
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107742975

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945593C>A , CM000665.2:g.138945593C>A GRCh38
NC_000003.11:g.138664435C>A , CM000665.1:g.138664435C>A GRCh37
NC_000003.10:g.140147125C>A NCBI36
NG_012454.1:g.6548G>T
NG_029796.1:g.3360C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.1130G>T MANE Select ENSP00000497217.1:p.Ter377Leu
ENST00000330315.3:c.1130G>T ENSP00000333188.3:p.Ter377Leu
NM_023067.3:c.1130G>T NP_075555.1:p.Ter377Leu
NM_023067.4:c.1130G>T MANE Select NP_075555.1:p.Ter377Leu