Canonical Allele Identifier: CA1405402037
Gene: FOXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.138945338A= , CM000665.2:g.138945338A= GRCh38
NC_000003.11:g.138664180A= , CM000665.1:g.138664180A= GRCh37
NC_000003.10:g.140146870A= NCBI36
NG_012454.1:g.6803T=
NG_029796.1:g.3105A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000648323.1:c.*254T= MANE Select ENSP00000497217.1:n.*254T=
ENST00000330315.3:c.*254T= ENSP00000333188.3:n.*254T=
NM_023067.3:c.*254T= NP_075555.1:n.*254T=
NM_023067.4:c.*254T= MANE Select NP_075555.1:n.*254T=