Canonical Allele Identifier: CA1405401768
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945467T= , CM000665.2:g.138945467T= GRCh38
NC_000003.11:g.138664309T= , CM000665.1:g.138664309T= GRCh37
NC_000003.10:g.140146999T= NCBI36
NG_012454.1:g.6674A=
NG_029796.1:g.3234T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*125A= MANE Select ENSP00000497217.1:n.*125A=
ENST00000330315.3:c.*125A= ENSP00000333188.3:n.*125A=
NM_023067.3:c.*125A= NP_075555.1:n.*125A=
NM_023067.4:c.*125A= MANE Select NP_075555.1:n.*125A=