Canonical Allele Identifier: CA1405401787
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945492T= , CM000665.2:g.138945492T= GRCh38
NC_000003.11:g.138664334T= , CM000665.1:g.138664334T= GRCh37
NC_000003.10:g.140147024T= NCBI36
NG_012454.1:g.6649A=
NG_029796.1:g.3259T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*100A= MANE Select ENSP00000497217.1:n.*100A=
ENST00000330315.3:c.*100A= ENSP00000333188.3:n.*100A=
NM_023067.3:c.*100A= NP_075555.1:n.*100A=
NM_023067.4:c.*100A= MANE Select NP_075555.1:n.*100A=