Canonical Allele Identifier: CA2704124030
Gene: FOXL2 HGNC NCBI

Linked Data

dbSNP Id: rs2107743576

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945967_138945978del , CM000665.2:g.138945967_138945978del GRCh38
NC_000003.11:g.138664809_138664820del , CM000665.1:g.138664809_138664820del GRCh37
NC_000003.10:g.140147499_140147510del NCBI36
NG_012454.1:g.6165_6176del
NG_029796.1:g.3734_3745del

Transcript Alleles

HGVS Amino-acid change
ENST00000648323.1:c.747_758del MANE Select ENSP00000497217.1:p.Gly250_Ala253del
ENST00000330315.3:c.747_758del ENSP00000333188.3:p.Gly250_Ala253del
NM_023067.3:c.747_758del NP_075555.1:p.Gly250_Ala253del
NM_023067.4:c.747_758del MANE Select NP_075555.1:p.Gly250_Ala253del