Canonical Allele Identifier: CA1405401772
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945469G= , CM000665.2:g.138945469G= GRCh38
NC_000003.11:g.138664311G= , CM000665.1:g.138664311G= GRCh37
NC_000003.10:g.140147001G= NCBI36
NG_012454.1:g.6672C=
NG_029796.1:g.3236G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*123C= MANE Select ENSP00000497217.1:n.*123C=
ENST00000330315.3:c.*123C= ENSP00000333188.3:n.*123C=
NM_023067.3:c.*123C= NP_075555.1:n.*123C=
NM_023067.4:c.*123C= MANE Select NP_075555.1:n.*123C=