Canonical Allele Identifier: CA1405402000
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945288C= , CM000665.2:g.138945288C= GRCh38
NC_000003.11:g.138664130C= , CM000665.1:g.138664130C= GRCh37
NC_000003.10:g.140146820C= NCBI36
NG_012454.1:g.6853G=
NG_029796.1:g.3055C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*304G= MANE Select ENSP00000497217.1:n.*304G=
ENST00000330315.3:c.*304G= ENSP00000333188.3:n.*304G=
NM_023067.3:c.*304G= NP_075555.1:n.*304G=
NM_023067.4:c.*304G= MANE Select NP_075555.1:n.*304G=