Canonical Allele Identifier: CA1405401775
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945470C= , CM000665.2:g.138945470C= GRCh38
NC_000003.11:g.138664312C= , CM000665.1:g.138664312C= GRCh37
NC_000003.10:g.140147002C= NCBI36
NG_012454.1:g.6671G=
NG_029796.1:g.3237C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*122G= MANE Select ENSP00000497217.1:n.*122G=
ENST00000330315.3:c.*122G= ENSP00000333188.3:n.*122G=
NM_023067.3:c.*122G= NP_075555.1:n.*122G=
NM_023067.4:c.*122G= MANE Select NP_075555.1:n.*122G=