Canonical Allele Identifier: CA1405402467
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138946333C= , CM000665.2:g.138946333C= GRCh38
NC_000003.11:g.138665175C= , CM000665.1:g.138665175C= GRCh37
NC_000003.10:g.140147865C= NCBI36
NG_012454.1:g.5808G=
NG_029796.1:g.4100C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.390G= MANE Select ENSP00000497217.1:p.Leu130=
ENST00000330315.3:c.390G= ENSP00000333188.3:p.Leu130=
NM_023067.3:c.390G= NP_075555.1:p.Leu130=
NM_023067.4:c.390G= MANE Select NP_075555.1:p.Leu130=