Canonical Allele Identifier: CA1405402588
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946597G= , CM000665.2:g.138946597G= GRCh38
NC_000003.11:g.138665439G= , CM000665.1:g.138665439G= GRCh37
NC_000003.10:g.140148129G= NCBI36
NG_012454.1:g.5544C=
NG_029796.1:g.4364G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.126C= MANE Select ENSP00000497217.1:p.Gly42=
ENST00000330315.3:c.126C= ENSP00000333188.3:p.Gly42=
NM_023067.3:c.126C= NP_075555.1:p.Gly42=
NM_023067.4:c.126C= MANE Select NP_075555.1:p.Gly42=